Surgi-Med, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K881705 | MODEL 5000 AIR-FLUIDIZED SUPPORT SYSTEM | INX | 1988-07-13 | View |
| 510(k) | K873047 | KEANE MOBILITY BED | IKZ | 1987-10-15 | View |
| 510(k) | K872923 | PARAGON 9000 TILT AND TURN BED | FNL | 1987-10-14 | View |
| 510(k) | K872924 | PARAGON 8500 CARDIO-PULMONARY BED | FNL | 1987-10-09 | View |
| 510(k) | K872925 | MEGABED 1000 | FNL | 1987-09-15 | View |
No matching devices.
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