510(k) K963120 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEM
| Applicant | Marquette Electronics, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Feb 28, 1997 |
| Received | Aug 12, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963120
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.