510(k) K121367 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
ZOLL PROPAQ XM
| Applicant | ZOLL Medical Corporation, Chelsmford MA, US |
| Decision | Substantially Equivalent, Jun 21, 2012 |
| Received | May 7, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121367
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 31, 2014 | ZOLL Medical Corporation Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Version 02.10.02.00 or Higher, automated external defibrillator. Terminated |
MKJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.