510(k) K943301 ยท DRX Electrode, Electrocardiograph
QUIK COMBO
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Feb 3, 1995 |
| Received | Jul 8, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943301
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.