510(k) K910754 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
MODEL 43100A SERIES DEFIBRILLATOR, MODIFICATION
| Applicant | Hewlett-Packard Co., Mcminnville OR, US |
| Decision | Substantially Equivalent, May 8, 1991 |
| Received | Feb 11, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910754
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.