ClearanceBrief
510(k) K083534 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

LIFEBED NETWORK PATIENT VIGILANCE SYSTEM

ApplicantHoana Medical, Inc., Honolulu HI, US
DecisionSubstantially Equivalent, Apr 13, 2009
ReceivedNov 28, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K083534

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.