ClearanceBrief
510(k) K860103 ยท GCP Endoscope, Ac-Powered And Accessories

MOD. ENDOPORT SINGLE-USE TROCAR AND SLEEVE

ApplicantEndotherapeutics, Redwood City CA, US
DecisionSubstantially Equivalent, Feb 12, 1986
ReceivedJan 10, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860103

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.