Survival Technology, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K925535 | CARDIOBEEPER(R) CB-IIA | DXH | 1993-01-28 | View |
| 510(k) | K894799 | CARDIOBEEPER MEMORY MONITOR CB 600 SERIES | DXH | 1989-10-03 | View |
| 510(k) | K890461 | CARDIOBEEPER IV | DXH | 1989-02-23 | View |
| 510(k) | K883843 | CARDIOBEEPER II | DXH | 1988-11-09 | View |
| 510(k) | K883614 | CYTOGUARD(R) | FMF | 1988-09-15 | View |
| 510(k) | K880300 | CARDIOBEEPER(R) III | DXH | 1988-05-12 | View |
| 510(k) | K844966 | CARDIOBEEPER PROFILE MONITOR | DXH | 1985-02-08 | View |
| 510(k) | K822093 | STAT-SCAN | DXG | 1982-09-21 | View |
| 510(k) | K813101 | CARDIOBEEPER MEMORY MONITOR | DXY | 1981-11-27 | View |
| 510(k) | K772178 | PACER MONITOR, PULSE WIDTH | DXH | 1977-12-08 | View |
No matching devices.
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