ClearanceBrief
510(k) K051594 ยท HEW Culdoscope (And Accessories)

MCCARTNEY ACCESS TUBE

ApplicantGynetech Pty. , Ltd., Cincinnati OH, US
DecisionSubstantially Equivalent, Sep 2, 2005
ReceivedJun 16, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051594

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.