ClearanceBrief
510(k) K082720 ยท EOQ Bronchoscope (Flexible Or Rigid)

TRACHEAL INTUBATION FIBERVIDEOSCOPE, MODELS LF-Y0004 AND LF-Y0005

ApplicantOlympus Medical Systems Corporation, Center Valley PA, US
DecisionSubstantially Equivalent, Nov 5, 2008
ReceivedSep 17, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082720

DateFirm and productCodeLinked 510(k)
Nov 17, 2023Aizu Olympus Co., Ltd.
Mobile airway scope-diagnosis and observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Numbers: MAF-DM2, MAF-GM, MAF-GM2, MAF-TM, MAF-TM2.
Open, Classified
EOQNone listed
Aug 31, 2023Olympus Corporation of the Americas
Olympus Airway Mobilescope, Models MAF-GM & MAF-TM.
Open, Classified
EOQNone listed
Aug 8, 2018Olympus Corporation of the Americas
Airway Mobilescope MAF-TM
Terminated
EOQNone listed

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