Phoenix Biomedical Corp.
FDA 510(k) & PMA Approved Devices — 12 products
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Total Devices12
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K030468 | ACURA ELITE GRAVITY COMPENSATING RESERVOIR | JXG | 2003-10-15 | View |
| 510(k) | K024101 | PHOENIX UNIVERSAL SHUNT SYSTEM | JXG | 2003-01-27 | View |
| 510(k) | K024040 | ACCURA ELITE SHUNT SYSTEM | JXG | 2003-01-27 | View |
| 510(k) | K021644 | PERF (OMMAYA STYLE) RESERVOIRS | JXG | 2002-08-06 | View |
| 510(k) | K002476 | LUMBOPERITONEAL SHUNT SYSTEM | JXG | 2000-11-09 | View |
| 510(k) | K000514 | RUMBAR DRAINAGE SYSTEM | JXG | 2000-05-10 | View |
| 510(k) | K991429 | DIAMOND II VALVE | JXG | 1999-05-19 | View |
| 510(k) | K990256 | CRX WORLD SHUNT | JXG | 1999-04-01 | View |
| 510(k) | K974096 | CRX DIAMOND VALVE | JXG | 1998-12-08 | View |
| 510(k) | K962144 | PHOENIX ETE TISSUE EXTENSION SYSTEM | MKY | 1997-01-14 | View |
| 510(k) | K960435 | PHOENIX CRX VALVE | JXG | 1996-08-27 | View |
| 510(k) | K953128 | SUTURE CORD | GAS | 1996-02-09 | View |
No matching devices.
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