510(k) K782079 ยท DRX Electrode, Electrocardiograph
ELECTRODE SYSTEM, QUIK-PREP
| Applicant | Quinton, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 1, 1979 |
| Received | Dec 13, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K782079
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.