510(k) K910634 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
DC200 DEFIBRILLATOR
| Applicant | Siemens Burdick, Inc., Miltoon WI, US |
| Decision | Substantially Equivalent, Jul 24, 1991 |
| Received | Feb 13, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910634
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.