Olympus Corporation of the Americas - FDA 510(k) Cleared Devices
Recent clearances: VISERA CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE V2, VISERA CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE VA2, VISERA CYSTO-NE
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Olympus Corporation of the Americas Gastroenterology & Urology ✕
1 devices