ClearanceBrief
510(k) K934023 ยท GCJ Laparoscope, General & Plastic Surgery

PHX TECHNOLOGIES CORP., ALTRAUMATIC GRASPER DEVICE

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

Recalls that name K934023

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.