510(k) K853732 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
LIFEPAK 8 MODIFICATION
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Dec 9, 1985 |
| Received | Sep 6, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853732
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.