510(k) K903018 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002
| Applicant | Medtronic Andover Medical, Inc., Haverhill MA, US |
| Decision | Substantially Equivalent, Dec 3, 1990 |
| Received | Jul 11, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903018
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.