ClearanceBrief
510(k) K934552 ยท HIR Perineometer

PERIPUMP

ApplicantDeschutes Medical Products, Inc., Bend OR, US
DecisionSubstantially Equivalent, Aug 9, 1995
ReceivedSep 21, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934552

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.