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. Ear, Nose, Throat ✕
3 devices
Cleared
Oct 16, 2003
EVIS EXERA BRONCHOFIBERVIDEOSCOPE OLYMPUS BF TYPE XP160F, ITS ACCESSORIES AND...
Ear, Nose, Throat
10d
Cleared
Jul 24, 2003
VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V
Ear, Nose, Throat
57d
Cleared
Dec 26, 2001
XENF-TP RHINO-LARYNGOFIBERSCOPE, ITS ACESSORIES AND ANCILLARY EQUIPMENT
Ear, Nose, Throat
57d