510(k) K110192 ยท DRL Tester, Defibrillator
DEFIBRILLATOR ANALYZER - DA-2006P
| Applicant | Bc Group International, Inc., Oak Grove MN, US |
| Decision | Substantially Equivalent, Feb 8, 2011 |
| Received | Jan 24, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110192
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 22, 2015 | BC Group International Inc DA-2006P - Defibrillator / Pacer Analyzer;
Product Usage:
Intended to measure the output of a defibrillator or transcutaneous pacemaker. Terminated |
DRL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.