The Olympus Optical Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
26
Inspections
0
Compliance Actions
0

Known Names

olympus optical co, olympus optical

Recent 510(k) Clearances

K-NumberDeviceDate
K032066SONOSURG SYSTEMOctober 3, 2003
K030194XUES-41 ENDOSCOPIC ELECTROSURGICAL UNITMarch 24, 2003
K021962OLYMPUS ULTRASONIC SURGICAL SYSTEMFebruary 12, 2003
K023984MODIFICATION TO OLYMPUS BRONCHOSCOPES BF-40 SERIES, BF-240 SERIES, AND BF-160 SERIESJanuary 31, 2003
K023272DISPOSABLE ASPIRATION NEEDLE NA-200HDecember 23, 2002
K023767UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIESNovember 29, 2002
K012074XBO1-824-18/19/20 BIOPSY FORCEPSSeptember 25, 2001
K012073OLYMPUS SPRAY CATHETER PW-6C-1August 10, 2001
K011869XENF-DP RHINO-LARYNGOFIBERSCOPE, ITS ACCESSORIES AND ANCILLARY EQUIPMENTJuly 25, 2001
K011151EVIS EXERA GASTROINTESTINAL VIDEOSCOPE GIF-Q160ZMay 15, 2001
K011149DISPOSABLE BENDING CANNULA PR-233QMay 15, 2001
K002749ENDOSCOPE CONTOUR DETECTION DEVICE, MODEL 3DX45 AND COLONOSCOPE, MODEL XCF-Q140L/13DDecember 4, 2000
K000095OLYMPUS SONOSURG TROCAR XT3900 SYSTEMSeptember 26, 2000
K001203OLYMPUS UM 2R/3R ULTRASONIC PROBE AND ASSOCIATED ANCILLARY EQUIPMENT FOR FEMALE REPRODUCTIVE TRACTMay 26, 2000
K001241EVIS EXERA COLONOVIDEOSCOPE CF-Q160 AL/I AND PCF-160 AL/IMay 9, 2000
K993041OLYMPUS XCYF-1T3 OES CYSTOFIBERSCOPE/NEPHROFIBERSCOPE ACCESSORIES AND ANCILLARY EQUIPMENTMarch 30, 2000
K990687HX-5/6-1 ENDOSCOPIC CLIPPING DEVICE, ENDOSCOPIC CLIPSMarch 26, 1999
K982610OLYMPUS UM-2R/3R ULTRASONIC PROBES AND ASSOCIATED ANCILLARY EQUIPMENT (URINARY TRACT)November 16, 1998
K982733OLYMPUS MH-246R BALLOON SHEATH, FOR BRONCHIAL USEOctober 28, 1998
K982133OLYMPUS ENDOSCOPIC SYSTEM LUMBAR HERNIA DISCECTOMY AND ITS ANCILLARY EQUIPMENTOctober 22, 1998