510(k) K871325 ยท DRX Electrode, Electrocardiograph
BOWEN REUSEABLE/DISPOSABLE ELECTRODE
| Applicant | Bowen & Company, Inc., Rockville MD, US |
| Decision | Substantially Equivalent, Jun 8, 1987 |
| Received | Apr 3, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871325
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.