ClearanceBrief
510(k) K890242 ยท GDZ Handle, Scalpel

SCALPEL HANDLE

ApplicantKinetic Medical Products, Erie PA, US
DecisionSubstantially Equivalent, Jan 27, 1989
ReceivedJan 18, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890242

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.