Plancon Instruments
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) | K980924 | PLANCON MICROLAMELLAR KERATOME EVOLUTION | HNO | 1998-04-15 | View |
| 510(k) | K970377 | PLANCON MICROLAMELLAR KERATOME (SINGLE PIECE KERATOME HEAD WITH ACCESSORIES) | HNO | 1997-03-31 | View |
| 510(k) | K960395 | PLANCON MIRCOLAMELLAR KERATOME | HNO | 1996-04-26 | View |
No matching devices.
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