510(k) K912835 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
MINI-PACK 911 SERIES
| Applicant | Pace Tech, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Feb 3, 1992 |
| Received | Jun 26, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912835
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.