Prodrive Systems, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K090369 | PRODRIVE LINE OF DENTAL HANDPIECES | EFB | 2009-02-27 | View |
| 510(k) | K073353 | DO-ALL DENTAL HANDPIECE LUBRICANT | EFB | 2007-12-07 | View |
| 510(k) | K062219 | PRODRIVE SYSTEMS REPLACEMENT TURBINE | EFB | 2006-08-04 | View |
No matching devices.
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