510(k) K841611 ยท DPS Electrocardiograph
QUINTON 901 & 900 HOLTER SCANNER
| Applicant | Quinton, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 2, 1984 |
| Received | Apr 3, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K841611
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.