510(k) K973639 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC.
| Applicant | J-Lloyd Medical, Inc., West Berlin NJ, US |
| Decision | Substantially Equivalent, Apr 20, 1998 |
| Received | Sep 24, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973639
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.