510(k) K810237 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
PORTABLE, BATTERY OPERATED DEFIBRILLATOR
| Applicant | Honeywell, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 19, 1981 |
| Received | Jan 28, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810237
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.