510(k) K863303 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
MODEL 617D
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Sep 5, 1986 |
| Received | Aug 25, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863303
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.