ClearanceBrief
510(k) K962212 ยท FDT Duodenoscope And Accessories, Flexible/Rigid

KARL STORZ FRIMBERGER VARIOGUIDE

ApplicantKARL STORZ Endoscopy-America, Inc., Culver City CA, US
DecisionSubstantially Equivalent, Dec 13, 1996
ReceivedJun 10, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962212

No recall in the FDA data names this 510(k).

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