ClearanceBrief
510(k) K895251 ยท KPN Alarm, Conditioned Response Enuresis

BARD INTRAVAGINAL STIM. KIT W/(IVES(TM))

ApplicantC.R. Bard, Inc., Covington GA, US
DecisionSubstantially Equivalent, Nov 13, 1989
ReceivedAug 21, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895251

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.