Medical Device Manufacturer · US , Melville , NY

The Olympus Optical Co. - FDA 510(k) Cleared Devices

22 submissions · 22 cleared · Since 1998

Recent clearances: SONOSURG SYSTEM, XUES-41 ENDOSCOPIC ELECTROSURGICAL UNIT, OLYMPUS ULTRASONIC SURGICAL SYSTEM

22
Total
22
Cleared
0
Denied

The Olympus Optical Co. has 22 FDA 510(k) cleared medical devices. Based in Melville, US.

Historical record: 22 cleared submissions from 1998 to 2003.

Browse the FDA 510(k) cleared devices submitted by The Olympus Optical Co. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.

FDA 510(k) Regulatory Record - The Olympus Optical Co.

22 devices
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