Olympus Corporation
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K072643 | CRYSTALEYE SPECTROPHOTOMETER/CRYSTALEYE BASIC SET, MODEL CE100-DC/US | KZN | 2007-11-16 | View |
| 510(k) | K043128 | OLYMPUS ENDOARM | GWG | 2004-12-21 | View |
| 510(k) | K042140 | OLYMPUS BF TYPE UC160-OL8 | ODG | 2004-08-18 | View |
| 510(k) | K041494 | OLYMPUS INTEGRATED ENDOSURGERY SYSTEM ENDOALPHA (CONTROL UNIT FOR ENDOSURGERY UCES-2) SOFTWARE VERSION 2 | FET | 2004-07-01 | View |
| 510(k) | K040940 | BRONCHOVIDEOSCOPE OLYMPUS XBF-D160HM | EOQ | 2004-04-19 | View |
No matching devices.
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