510(k) K903437 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
DISPOS ACCESS EXTERNAL CARDIAC PACEMAKER
| Applicant | Keller Medical Specialties Products, Inc., Antioch IL, US |
| Decision | Substantially Equivalent, Nov 16, 1990 |
| Received | Jul 31, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903437
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.