Kaltenbach & Voigt GmbH & Co.
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) | K092446 | INTRA LUX HEAD 3 LDSY | EFA | 2009-11-03 | View |
| 510(k) | K080677 | COMFORTRONIC 4894 AND COMFORTDRIVE 200XDA HANDPIECE | EIA | 2008-06-06 | View |
No matching devices.
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