ClearanceBrief
510(k) K003576 ยท DSI Detector And Alarm, Arrhythmia

Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503

ApplicantQuinton, Inc., Bothell WA, US
DecisionSubstantially Equivalent, Jan 25, 2001
ReceivedNov 20, 2000
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K003576

DateFirm and productCodeLinked 510(k)
Jun 4, 2010Cardiac Science Corporation
Treadmill models TM55, TM65, and CR60 (brand names include Quinton, Burdick, and Cardiac Science).
Terminated
IOLNone listed

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