Olympus Corporation - FDA 510(k) Cleared Devices
Recent clearances: CRYSTALEYE SPECTROPHOTOMETER/CRYSTALEYE BASIC SET, MODEL CE100-DC/US, OLYMPUS ENDOARM, OLYMPUS BF TYPE UC160-OL8
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Olympus Corporation Neurology ✕
1 devices