510(k) K954957 ยท MKJ Automated External Defibrillators (Non-Wearable)
CODEMASTER XL + XL W/SHOCK ADVISORY OPTION
| Applicant | Hewlett-Packard Co., Mcminnville OR, US |
| Decision | Substantially Equivalent, May 7, 1996 |
| Received | Oct 27, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954957
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.