Company ยท US
Surgipath Medical Industries, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1988. Name variants (Inc, Corp, punctuation) are merged.
30510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| IFP | Formalin, Neutral Buffered | 4 |
| HHT | Spatula, Cervical, Cytological | 3 |
| KEO | Formulations, Paraffin, All | 3 |
| IDL | Microtome, Accessories | 2 |
| IDZ | Cassettes, Tissue | 2 |
| KER | Container, Embedding | 2 |
| EMF | Knife, Surgical | 1 |
| HZT | Reagent, Schiff | 1 |
| IAB | Toluidine Blue | 1 |
| IDO | Microtome, Rotary | 1 |
| IER | Polyethylene Glycol (Carbowax) | 1 |
| IFZ | Gelatin For Specimen Adhesion | 1 |
| IGG | Formaldehyde (Formalin, Formol) | 1 |
| KDX | Solution, Decalcifier, Acid Containing | 1 |
| KEM | Agent, Clearing | 1 |
| KEP | Media, Mounting, Oil Soluble | 1 |
| KEQ | Media, Mounting, Water Soluble | 1 |
| LDZ | Fixative, Alcohol Containing | 1 |
| LEA | Preservative, Cytological | 1 |
| PPM | General Purpose Reagent | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 5, 1988 | K883217 | SCHIFF REAGENT Surgipath Medical Industries, Inc. | HZT |
| Jul 19, 1988 | K881921 | C-E BRUSH Surgipath Medical Industries, Inc. | HHT |
| May 25, 1988 | K881922 | CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE Surgipath Medical Industries, Inc. | LDZ |
| Apr 21, 1988 | K881659 | TISSUE SECTION ADHESIVE Surgipath Medical Industries, Inc. | IFZ |
| Sep 30, 1986 | K863549 | REUSABLE/DISPOSABLE AUTOPSY KNIFE SET Surgipath Medical Industries, Inc. | EMF |
| Sep 25, 1986 | K863616 | KNIFE MAKER Surgipath Medical Industries, Inc. | IDL |
| Sep 19, 1986 | K863548 | ROTARY MICROTOME Surgipath Medical Industries, Inc. | IDO |
| Sep 16, 1986 | K863483 | CASSETTE EMBOSSEER Surgipath Medical Industries, Inc. | IDZ |
| Aug 19, 1986 | K863145 | CERVICAL SCRAPERS Surgipath Medical Industries, Inc. | HHT |
| Apr 11, 1986 | K861270 | BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED. Surgipath Medical Industries, Inc. | KEO |
| Apr 11, 1986 | K861201 | FORMALDEHYDE SOLUTION, 37% Surgipath Medical Industries, Inc. | IGG |
| Jan 7, 1986 | K855109 | CLEARENE, CLEARING AGENT Surgipath Medical Industries, Inc. | KEM |
| Aug 28, 1985 | K853497 | PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALIN Surgipath Medical Industries, Inc. | IFP |
| Jun 10, 1985 | K852045 | SED-FIX CONCENTRATE Surgipath Medical Industries, Inc. | IER |
| Mar 25, 1985 | K850916 | SPRAYFIX Surgipath Medical Industries, Inc. | PPM |
| Mar 22, 1985 | K850676 | SURGI-PAP KIT Surgipath Medical Industries, Inc. | HHT |
| Jan 30, 1985 | K844640 | POLYSTAT, BIOLOGICAL STAIN Surgipath Medical Industries, Inc. | IAB |
| May 2, 1984 | K841488 | DECALCIFIER I Surgipath Medical Industries, Inc. | KDX |
| Jun 17, 1983 | K831580 | PARAFFIN INFILTRATION MEDIUM Surgipath Medical Industries, Inc. | KEO |
| May 25, 1983 | K831334 | TISSUE CASSETTES FOR PROCESSING-EM BED Surgipath Medical Industries, Inc. | IDZ |
| May 25, 1983 | K831333 | EMBEDDING RINGS Surgipath Medical Industries, Inc. | KER |
| May 16, 1983 | K831335 | DISPOSABLE BASE MOLD Surgipath Medical Industries, Inc. | KER |
| May 16, 1983 | K831308 | DISPOSABLE MICROTOME BLADE Surgipath Medical Industries, Inc. | IDL |
| Mar 31, 1983 | K830515 | SCOTTS TAP WATER SUBSTITUTE CONCENTRATE Surgipath Medical Industries, Inc. | KEQ |
| Mar 17, 1983 | K830659 | CLEARIUM, MOUNTING MEDIUM Surgipath Medical Industries, Inc. | KEP |
| Mar 17, 1983 | K830583 | NEUTRAL BUFFERED FORMALIN 10% Surgipath Medical Industries, Inc. | IFP |
| Mar 17, 1983 | K830582 | MILLONIG'S MODIFIED PHOSPHATE BUFFERED Surgipath Medical Industries, Inc. | IFP |
| Mar 8, 1983 | K830514 | MILLONIGS MODIFIED PHOSPHATE BUFFERED Surgipath Medical Industries, Inc. | IFP |
| Mar 17, 1981 | K810568 | PARAFFIN EMBEDDING MEDIUM Surgipath Medical Industries, Inc. | KEO |
| May 20, 1977 | K770592 | CYTOLOGY FIXATIVE Surgipath Medical Industries, Inc. | LEA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||