ClearanceBrief
510(k) K955661 ยท LDQ

ACU-HALT

ApplicantGlederer & Co., Inc., Paterson NJ, US
DecisionSubstantially Equivalent, Dec 30, 1996
ReceivedDec 12, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K955661

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.