ClearanceBrief
510(k) K992480 ยท HET Laparoscope, Gynecologic (And Accessories)

MEDIFIX SINGLE AND DOUBLE PUNCTURE LAPAROSCOPES

ApplicantMedifix, Inc., Morton Grove IL, US
DecisionSubstantially Equivalent, Sep 23, 1999
ReceivedJul 26, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992480

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.