ClearanceBrief
510(k) K221631 ยท EOQ Bronchoscope (Flexible Or Rigid)

Tracheal Intubation Fiberscope OLYMPUS LF-P, VISERA Tracheal Intubation Videoscope OLYMPUS LF Type V

ApplicantOlympus Medical Systems Corp., Tokyo, JP
DecisionSubstantially Equivalent, Sep 26, 2022
ReceivedJun 6, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221631

DateFirm and productCodeLinked 510(k)
Nov 17, 2023Aizu Olympus Co., Ltd.
Tracheal videoscope- For airway management, which includes observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Number: LF-V.
Open, Classified
EOQNone listed
Aug 31, 2023Olympus Corporation of the Americas
Olympus Tracheal Intubation Fiberscope, Models LF-P & LF-V.
Open, Classified
EOQNone listed
Aug 4, 2023Olympus Corporation of the Americas
VISERA Tracheal Intubation Videoscope OLYMPUS LF Type V- For airway management which includes endoscopic observation to access airway anatomy, endotracheal/endobronchial intubation and management.
Open, Classified
EOQNone listed
Aug 4, 2023Olympus Corporation of the Americas
Tracheal Intubation Fiberscope OLYMPUS LF-P- To be used with an Olympus Light Source, documentation equipment, display monitor and other ancillary equipment for management of Endotracheal Tube
Open, Classified
EOQNone listed

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