ClearanceBrief
510(k) K101109 ยท KMI Monitor, Bed Patient

VIVATRAK

ApplicantWireless Medcare, LLC, Marietta GA, US
DecisionSubstantially Equivalent, Jul 15, 2010
ReceivedApr 20, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K101109

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.