ClearanceBrief
510(k) K921019 ยท GAD Retractor

HARGIS RECTAL SELF RETRATION SYSTEM

ApplicantMedin Corp., Wallington NJ, US
DecisionSubstantially Equivalent, Jul 2, 1993
ReceivedMar 3, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921019

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.