510(k) K915757 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
MODELS M1722A, M1723A, M1724A DEFIBRILLATORS
| Applicant | Hewlett-Packard Co., Mcminnville OR, US |
| Decision | Substantially Equivalent, Jul 30, 1992 |
| Received | Dec 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915757
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.