ClearanceBrief
510(k) K072996 ยท BZD Ventilator, Non-Continuous (Respirator)

REMSTAR PRO M-SERIES CPAP & HEATED HUMIDIFIER SYSTEM

ApplicantRespironics, Inc., Murrysville PA, US
DecisionSubstantially Equivalent, Dec 27, 2007
ReceivedOct 24, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K072996

DateFirm and productCodeLinked 510(k)
Jun 17, 2009Respironics
Remstar Pro M-Series Heated Humidifier System.
Terminated
BZDNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.