Company ยท US
American Heyer Schulte
FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1984. Name variants (Inc, Corp, punctuation) are merged.
13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| JXG | Shunt, Central Nervous System And Components | 4 |
| GCY | Apparatus, Suction, Single Patient Use, Portable, Nonpowered | 2 |
| GDW | Staple, Implantable | 2 |
| FTL | Mesh, Surgical, Polymeric | 1 |
| IWJ | System, Applicator, Radionuclide, Manual | 1 |
| JCY | Catheter, Infusion | 1 |
| LCJ | Tissue Expander And Accessories | 1 |
| LKG | Port & Catheter, Implanted, Subcutaneous, Intraventricular | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 27, 1984 | K840172 | VENTRAL WALL DEFECT REDUCT SILO American Heyer Schulte | FTL |
| Apr 3, 1984 | K834593 | ONE-PIECE SHUNT American Heyer Schulte | JXG |
| Feb 3, 1984 | K833502 | RADOVAN SUBCUTANEOUS TISSUE EXPANDER American Heyer Schulte | LCJ |
| Jan 25, 1984 | K833698 | AMER. V. MUELLER SURG. STAPLES ILA American Heyer Schulte | GDW |
| Dec 29, 1983 | K833704 | AMER. V. MUELLER SURGICALSTAPLES-CARTR American Heyer Schulte | GDW |
| Sep 29, 1983 | K832738 | HEYER-SCHULTE AFTERLOADING CATHETER American Heyer Schulte | IWJ |
| Apr 28, 1983 | K823790 | VENTRICULAR ACCESS SYSTEM American Heyer Schulte | LKG |
| Apr 12, 1983 | K822096 | CHEMOTHERAPY INFUSION CATHETER American Heyer Schulte | JCY |
| Aug 16, 1982 | K822032 | LARGE VOLUME CLOSED WOUND SUCTION DRAIN American Heyer Schulte | GCY |
| Feb 18, 1982 | K820247 | EXTERNAL VENTRICULAR DRAINAGE SYS. American Heyer Schulte | JXG |
| Jun 26, 1981 | K811288 | SPETZLER LUMBAR-PERITONEAL SYSTEM American Heyer Schulte | JXG |
| Dec 18, 1980 | K802586 | AMERICAN HEYER-SCHULTE LOW PROFILE VALVE American Heyer Schulte | JXG |
| Aug 20, 1980 | K801766 | JACKSON-PRATT LARGE VOL. CLOSED WOUND American Heyer Schulte | GCY |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||