510(k) K073230 ยท DTA Tester, Pacemaker Electrode Function
MODELS ERA 300 AND 3105 PACING SYSTEM ANALYZERS
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Dec 20, 2007 |
| Received | Nov 15, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K073230
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.