510(k) K953651 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER SYSTEM
| Applicant | Arrow Intl., Inc., Reading PA, US |
| Decision | Substantially Equivalent, Nov 30, 1995 |
| Received | Aug 4, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953651
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.