Company ยท US
Schiff & Co.
FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1999. Name variants (Inc, Corp, punctuation) are merged.
15510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| FRA | Purifier, Air, Ultraviolet, Medical | 2 |
| LYR | Helicobacter Pylori | 2 |
| BTM | Ventilator, Emergency, Manual (Resuscitator) | 1 |
| DHA | System, Test, Human Chorionic Gonadotropin | 1 |
| DTN | Reservoir, Blood, Cardiopulmonary Bypass | 1 |
| DZM | Needle, Dental | 1 |
| FOS | Catheter, Umbilical Artery | 1 |
| FPD | Tube, Feeding | 1 |
| GMI | Antigen, Cf And / Or Id, Coccidioides Immitis | 1 |
| JJQ | Colorimeter, Photometer, Spectrophotometer For Clinical Use | 1 |
| JKA | Tubes, Vials, Systems, Serum Separators, Blood Collection | 1 |
| JQW | Station, Pipetting And Diluting, For Clinical Use | 1 |
| KHE | Reagent, Occult Blood | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Apr 27, 1999 | K990511 | X-TIP INTRAOSSEOUS PERFORATOR Schiff & Co. | DZM |
| Mar 24, 1999 | K982136 | JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200 Schiff & Co. | DTN |
| Feb 4, 1999 | K981629 | NUTRISAFE ENTERAL FEEDING TUBE Schiff & Co. | FPD |
| Oct 1, 1998 | K981630 | VYGON DOUBLE LUMEN UMBILICAL CATHETER Schiff & Co. | FOS |
| May 21, 1998 | K974141 | PLUS REUSABLE RESUSCITATOR Schiff & Co. | BTM |
| Oct 28, 1996 | K954448 | VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM Schiff & Co. | FRA |
| Feb 9, 1996 | K955085 | HM-CAP EIA TEST (MODIFICATION) Schiff & Co. | LYR |
| Jul 18, 1995 | K944159 | HM-CAP EIA KIT Schiff & Co. | LYR |
| Feb 14, 1995 | K943521 | VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE Schiff & Co. | FRA |
| Apr 16, 1990 | K896684 | KEMBLE LIQUID HANDLING SYSTEM DISPENSER Schiff & Co. | JQW |
| Oct 31, 1989 | K894617 | OLYMPUS PK-TP SYSTEM REACTIVE CONTROL Schiff & Co. | GMI |
| Oct 30, 1989 | K895967 | FASTEC 901 AGGLUTINATION PATTERN READER Schiff & Co. | JJQ |
| Aug 8, 1988 | K882539 | CLEANTECH SYSTEM Schiff & Co. | JKA |
| May 13, 1988 | K874482 | REVISED IMMUDIA HEM-SP Schiff & Co. | KHE |
| Feb 2, 1988 | K873986 | BETA-HCG ASSAY Schiff & Co. | DHA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||