510(k) K973663 ยท DRX Electrode, Electrocardiograph
PALJET-B
| Applicant | Golden Gate Bio-Device, Castro Valley CA, US |
| Decision | Substantially Equivalent, Feb 10, 1998 |
| Received | Sep 25, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973663
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.