ClearanceBrief
510(k) K963648 ยท GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered

STRYKER SUCTION REGULATOR

ApplicantStryker Endoscopy, Santa Clara CA, US
DecisionSubstantially Equivalent, Nov 26, 1996
ReceivedSep 12, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963648

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.