ClearanceBrief
510(k) K821999 ยท GCP Endoscope, Ac-Powered And Accessories

ENDOSCOPIC SCLEROTHERAPY BALLOON

ApplicantRetech, Mchenry IL, US
DecisionSubstantially Equivalent, Aug 27, 1982
ReceivedJul 7, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821999

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.