510(k) K062099 ยท DRL Tester, Defibrillator
PHASE 3, MODEL DT-1
| Applicant | Datrend Systems, Inc., Richmond, British Columbia, CA |
| Decision | Substantially Equivalent, Jan 25, 2007 |
| Received | Jul 24, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062099
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.