510(k) K903657 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
MODEL 610 MODIFIED
| Applicant | First Medical Devices Corp., Kirkland WA, US |
| Decision | Substantially Equivalent, Sep 4, 1990 |
| Received | Aug 9, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903657
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.