510(k) K922742 ยท KRE Analyzer, Pacemaker Generator Function, Indirect
HPM 40 HEART PACEMAKER MONITOR
| Applicant | Biotronik, GmbH & Co., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Mar 18, 1993 |
| Received | Jun 8, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922742
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.