ClearanceBrief
510(k) K102219 ยท GCJ Laparoscope, General & Plastic Surgery

SOCORRO SMI TUNNEL RELEASE DEVICE

ApplicantSocorro Medical, Inc., San Francisco CA, US
DecisionSubstantially Equivalent, Sep 24, 2010
ReceivedAug 6, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K102219

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.