ClearanceBrief
510(k) K760778 ยท GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered

T-TUBE DRAIN, ROUND

ApplicantHeyer Schulte Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 3, 1976
ReceivedOct 4, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760778

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.