ClearanceBrief
510(k) K863162 ยท

VACU-GUARD

ApplicantArbor Technologies, Inc., Ann Arbor MI, US
DecisionSubstantially Equivalent, Aug 29, 1986
ReceivedAug 18, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863162

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.