510(k) K800937 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
R2 PLATE TYPE CABLE-ADAPTOR #S 175,176
| Applicant | R2 Corp., Walker MI, US |
| Decision | Substantially Equivalent, May 23, 1980 |
| Received | Apr 21, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800937
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.