ClearanceBrief
510(k) K910449 ยท KCY Tourniquet, Pneumatic

PRESTITCH

ApplicantCrantec Co., Salt Lake City UT, US
DecisionSubstantially Equivalent, May 29, 1992
ReceivedJan 29, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910449

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.