510(k) K182905 ยท DRL Tester, Defibrillator
UniPulse
| Applicant | Seaward Group, Peterlee, GB |
| Decision | Substantially Equivalent, Dec 14, 2018 |
| Received | Oct 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182905
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.