510(k) K881643 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
BATTERY PACKS FOR CARDIOVASCULAR UNITS
| Applicant | Dowit Service Co., Inc., Towaco NJ, US |
| Decision | Substantially Equivalent, May 17, 1988 |
| Received | Apr 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881643
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.