Olympus Optical Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: EVIS EXERA BRONCHOFIBERVIDEOSCOPE OLYMPUS BF TYPE XP160F, ITS ACCESSORIES AND ANCILLARY EQUIPMENT, OLYMPUS ULTRASONIC SURGICAL SYSTEM, VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V
22
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Olympus Optical Co., Ltd. Neurology ✕
1 devices