Olympus Corp of America
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) | K984255 | OLYMPUS HX-20 SERIES LIGATING DEVICE | MND | 1999-01-12 | View |
| 510(k) | K944250 | UREA NITROGEN REAGENT | CDQ | 1995-02-08 | View |
No matching devices.
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