ClearanceBrief
510(k) K112680 ยท FDF Colonoscope And Accessories, Flexible/Rigid

EVIS EXERA III VIDEO SYSTEM

ApplicantOlympus Medical Systems Corporation, Center Valley PA, US
DecisionSubstantially Equivalent, Feb 16, 2012
ReceivedSep 14, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K112680

DateFirm and productCodeLinked 510(k)
Feb 29, 2024Olympus Corporation of the Americas
Colonoscope, Model Number CF-HQ190I.
Open, Classified
FDFNone listed
Feb 29, 2024Olympus Corporation of the Americas
Colonoscope, Model Number CF-HQ190L.
Open, Classified
FDFNone listed
Feb 29, 2024Olympus Corporation of the Americas
Colonoscope, Model Number PCF-H190L.
Open, Classified
FDFNone listed
Nov 17, 2023Aizu Olympus Co., Ltd.
Colonoscope: for endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum, sigmoid colon, colon and ileocecal valve). Model Numbers: CF-2T160I, CF-2T160L, CF-H170
Open, Classified
FETNone listed
Nov 17, 2023Aizu Olympus Co., Ltd.
Gastrointestinal videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model Numbers: GIF-1TH190, GIF-1TQ160, GIF-2T160, GIF-2TH180, GIF-H170
Open, Classified
FDFNone listed
Nov 9, 2023Olympus Corporation of the Americas
EVIS EXERA III Gastrointestinal Videoscope
Open, Classified
FDFNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.