Company ยท US
American V. Mueller
FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1987. Name variants (Inc, Corp, punctuation) are merged.
31510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| GAG | Stapler, Surgical | 3 |
| JXG | Shunt, Central Nervous System And Components | 3 |
| DWS | Instruments, Surgical, Cardiovascular | 2 |
| EWL | Prosthesis, Laryngeal (Taub) | 2 |
| GAD | Retractor | 2 |
| KNA | Instrument, Manual, Specialized Obstetric-Gynecologic | 2 |
| ENW | Catheter, Nasopharyngeal | 1 |
| FZP | Clip, Implantable | 1 |
| GCY | Apparatus, Suction, Single Patient Use, Portable, Nonpowered | 1 |
| GDT | Staple, Removable (Skin) | 1 |
| GEF | Applier, Staple, Surgical, | 1 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 1 |
| GYK | Instrument, Shunt System Implantation | 1 |
| GZX | Instrument, Microsurgical | 1 |
| HAO | Instrument, Surgical, Non-Powered | 1 |
| HMX | Cannula, Ophthalmic | 1 |
| HND | Spatula, Ophthalmic | 1 |
| HNR | Forceps, Ophthalmic | 1 |
| KAE | Forceps, Ent | 1 |
| KNT | Tubes, Gastrointestinal (And Accessories) | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Dec 18, 1987 | K873771 | HEYER-SCHULTE(R) ONE PIECE SHUNT VENT. CATH. INTRO American V. Mueller | GYK |
| Sep 8, 1987 | K873332 | MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM American V. Mueller | GCY |
| Jun 12, 1987 | K871685 | HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS American V. Mueller | JXG |
| Dec 29, 1986 | K864676 | HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM American V. Mueller | JXG |
| Aug 18, 1986 | K862772 | V. MUELLER (R) GOOSENECK CIRCULAR STAPLER American V. Mueller | GAG |
| Jun 6, 1986 | K861471 | V. MUELLER VITAL CLIP-HEMOSTATIC CLIP American V. Mueller | FZP |
| Dec 2, 1985 | K854568 | V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP American V. Mueller | GEF |
| Nov 27, 1985 | K854049 | HEYER-SCHULTE SYRINGO PERITONEAL SHUNT American V. Mueller | JXG |
| Jul 22, 1985 | K851082 | V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES American V. Mueller | ENW |
| Jun 11, 1985 | K851974 | V. MUELLER VITAL SKIN STAPLER American V. Mueller | GDT |
| Apr 17, 1985 | K850947 | V-MUELLER INVERTED LINEAR ANASTOMOSIS INSTRUMENTS American V. Mueller | GAG |
| Dec 14, 1984 | K844628 | V. MUELLER PHEUMO-INTESTINAL INSTRUMENT SET American V. Mueller | GAG |
| Oct 11, 1984 | K843392 | GAUDERER GASTROSTOMY BUTTON American V. Mueller | KNT |
| Aug 17, 1984 | K842896 | BLOM-SINGER LOW PRESSURE VOICE PROSTHES American V. Mueller | EWL |
| Mar 6, 1984 | K840982 | LASER MIRROR American V. Mueller | |
| Dec 23, 1983 | K832967 | DUCKBILL VOICE PROSTHESIS & TRACHEO American V. Mueller | EWL |
| Jul 7, 1983 | K831455 | LEATHER VALVE CUTTER American V. Mueller | DWS |
| Apr 27, 1983 | K830532 | ELECTROSURGICAL CAULTERY PENCIL American V. Mueller | GEI |
| Jan 18, 1983 | K823792 | QUARTZ RETRACTOR/PROBE American V. Mueller | KOH |
| May 27, 1982 | K821569 | LEATHER VALVULOTOME American V. Mueller | DWS |
| Nov 2, 1981 | K812895 | YARMO NASAL CARTILAGE SOFTENER American V. Mueller | KAE |
| Jul 20, 1981 | K811759 | RETRACTING PROBES American V. Mueller | GAD |
| Jun 26, 1981 | K811658 | ANIS LENS IMPLANT FORCEPS #2 American V. Mueller | HNR |
| Jun 16, 1981 | K811455 | ANIS GUIDING CANNULA American V. Mueller | HMX |
| May 15, 1981 | K810937 | ANIS IRRIGATING SPATULA American V. Mueller | HND |
| Mar 11, 1981 | K810533 | CIRCLE NEPHROSTOMY TUBE INTRODUCER American V. Mueller | KOA |
| Mar 11, 1981 | K810484 | OVARY FORCEPS American V. Mueller | KNA |
| Mar 11, 1981 | K810483 | FALLOPIAN TUBE FORCEPS American V. Mueller | KNA |
| Feb 27, 1981 | K810485 | DUJOVNY MICROSURGICAL SCISSORS American V. Mueller | GZX |
| Sep 9, 1980 | K801760 | FIELD-LEE BRAIN BIOPSY NEEDLE American V. Mueller | HAO |
| Aug 20, 1980 | K801759 | EFFRON PAROTID RETRACTOR American V. Mueller | GAD |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||