510(k) K910291 ยท DSI Detector And Alarm, Arrhythmia
MODEL 43420B NEWWAVE HOLTER SYSTEM/MODIFICATION
| Applicant | Hewlett-Packard Co., Mcminnville OR, US |
| Decision | Substantially Equivalent, Apr 22, 1991 |
| Received | Jan 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910291
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.