Gorman Rupp Industries
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K771537 | AQUAMATIC K-MODULE MODEL K-20 | DWJ | 1977-09-06 | View |
| 510(k) | K770839 | AQUAMATIC K-77 | DWJ | 1977-06-08 | View |
| 510(k) | K770232 | BLOOD/FLUID WARMER MODEL DW-1000A | BSB | 1977-02-14 | View |
| 510(k) | K761337 | AQUAMATIC K-MODULE MODEL K-10 | JRR | 1977-01-10 | View |
| 510(k) | K760910 | DISPOSABLE K-PADS | ILO | 1976-12-16 | View |
| 510(k) | K761087 | ELECTRONIC CONTROL UNIT | DWJ | 1976-12-06 | View |
No matching devices.
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