ClearanceBrief
510(k) K942002 ยท GAD Retractor

RETRACTOR

ApplicantAutomated Medical Products Corp., New York NY, US
DecisionSubstantially Equivalent, May 17, 1994
ReceivedApr 25, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942002

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.