Dermanetics Corp.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K894723 | SYSTEM 2500 MEDICAL WATERBED | IOQ | 1989-08-17 | View |
| 510(k) | K890935 | SYSTEM 3000 FLUIDIZED AIR BED | IOQ | 1989-03-15 | View |
No matching devices.
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