ClearanceBrief
510(k) K832010 ยท EOQ Bronchoscope (Flexible Or Rigid)

BRONCHO-FIBERSCOPE

ApplicantKARL STORZ Endoscopy-America, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 1, 1983
ReceivedJun 23, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832010

DateFirm and productCodeLinked 510(k)
Dec 17, 2013Karl Storz Endoscopy America Inc
Broncho Flexible Fiberscope, models: 11001BN1, 11002BD1, 11004BC1, and 11009BC1. " Examination and treatment of the tracheobronchial tree Contraindications for Bronchoscopy " Uncontrolled angina, unc
Terminated
ECQNone listed

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