Schwind Eye-Tech-Solutions GmbH & Co. KG
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) | K082043 | CARRIAZO-PENDULAR MICROKERATOME | HNO | 2008-08-01 | View |
| 510(k) | K032910 | CARRIAZO PENDULAR | HNO | 2004-08-30 | View |
No matching devices.
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