ClearanceBrief
510(k) K041607 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

QUINTON Q-TE; RMS

ApplicantQuinton Cardiology, Inc., Bothell WA, US
DecisionSubstantially Equivalent, Jul 16, 2004
ReceivedJun 15, 2004
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K041607

DateFirm and productCodeLinked 510(k)
Apr 29, 2020WELCH ALLYN, INC/MORTARA
Q-Tel. The Q-Tel RMS system is a computer-based cardiac and pulmonary rehabilitation data acquisition and editing system.
Terminated
DPSNone listed

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