Cutter Laboratories, Inc.
FDA 510(k) & PMA Approved Devices — 39 products
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Total Devices39
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K861315 | HYPERBARIC PENETRATION EXTENSION SET | CBF | 1986-05-21 | View |
| 510(k) | K854106 | BAYSILEX | ELW | 1986-03-17 | View |
| 510(k) | K842324 | PERFOURM | ELW | 1984-11-09 | View |
| 510(k) | K834106 | INTRAVENOUS INFUSION CONTROLLER | LDR | 1984-05-30 | View |
| 510(k) | K832237 | ORTHOPEDIC CASTING TAPE MAXCAST | ITG | 1983-08-16 | View |
| 510(k) | K823214 | DOSIMETRIC RELEASE PROGRAM - ADMIN. SET | FPA | 1983-01-12 | View |
| 510(k) | K821326 | CUTTER BOND POLYCARBOXYLATE CEMENT | EMA | 1982-05-28 | View |
| 510(k) | K813532 | CUTTERBOND ZINC PHOSPHATE CEMENT | EMA | 1982-03-02 | View |
| 510(k) | K802104 | C-SPLINT | IQI | 1980-09-16 | View |
| 510(k) | K802105 | C-BLADE | HWE | 1980-09-16 | View |
| 510(k) | K801652 | TOTAL PARENTERAL NUTRITION SET BAG | KPE | 1980-08-27 | View |
| 510(k) | K801651 | CUTTER JET | EFB | 1980-08-13 | View |
| 510(k) | K800213 | PHARMACY ADDITIVE SYRINGE SET | KYW | 1980-02-26 | View |
| 510(k) | K792250 | CUTTER POINTS | EHL | 1980-01-23 | View |
| 510(k) | K792207 | PERIDIAL PERITONEAL DIALYSIS TRAY | FKG | 1979-12-10 | View |
| 510(k) | K790125 | ULNAR HEAD PROTHESIS | KXE | 1979-02-08 | View |
| 510(k) | K781937 | PROTHESIS, METACARPAL | 1979-01-17 | View | |
| 510(k) | K781521 | CUTTER RESIFLEX URINE METER | KNX | 1978-11-22 | View |
| 510(k) | K781668 | GAMMA RADIATION STERILIZATION PRECEDURE | KYJ | 1978-11-03 | View |
| 510(k) | K781059 | CUTTER/COMPUR MINI CENTRIFUGE | GKF | 1978-08-14 | View |
No matching devices.
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