510(k) K043361 ยท DRX Electrode, Electrocardiograph
ACCUHEART ELECTRODE BELT
| Applicant | Advanced Bioelectric Corporation, Montreal, Qc, CA |
| Decision | Substantially Equivalent, Mar 22, 2005 |
| Received | Dec 7, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043361
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.