510(k) K970481 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
V2
| Applicant | Survivalink Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jul 1, 1997 |
| Received | Feb 10, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970481
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.