ClearanceBrief
510(k) K941252 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

RESPIRATORY AND CARDIAC SPECTRAL FREQUENCY SIGNAL PROCESSOR

ApplicantAnsar, Philidelphia PA, US
DecisionSubstantially Equivalent, Sep 20, 1995
ReceivedMar 15, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K941252

DateFirm and productCodeLinked 510(k)
Aug 19, 2014Ansar Group, Inc. Dba Ansar Medical Technologies, Inc
Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor system. The ANX 3.0 system is comprised of these components. 1. Patient Physiological Monitor, 2. Laptop Computer, 3. Stand w/wheel
Terminated
DRTNone listed

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