ClearanceBrief
510(k) K082436 ยท HIR Perineometer

EXTT-101

ApplicantApimeds, Inc., Greenwood Village CO, US
DecisionSubstantially Equivalent, May 29, 2009
ReceivedAug 25, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082436

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.