ClearanceBrief
510(k) K905836 ยท IRO Vibrator, Therapeutic

ULTRA WAVE 101

ApplicantAko USA, Inc., Irving TX, US
DecisionSubstantially Equivalent, Jan 14, 1991
ReceivedDec 31, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905836

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.