510(k) K072114 ยท DRL Tester, Defibrillator
IMPULSE 6000D/7000DP
| Applicant | Fluke Biomedical, Orange CA, US |
| Decision | Substantially Equivalent, Jan 28, 2008 |
| Received | Aug 1, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072114
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.