ClearanceBrief
510(k) K934022 ยท GCJ Laparoscope, General & Plastic Surgery

PHX TECH SINGLE ACTION HEAVY-TOOTH JAW CLAW GRASPER

ApplicantPhx Technologies Corp., Lewisville TX, US
DecisionSubstantially Equivalent, Dec 17, 1993
ReceivedAug 17, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934022

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.