510(k) K941351 ยท DQA Oximeter
BURDICK PRO2 OXIMETER
| Applicant | Burdick Corp., Miltoon WI, US |
| Decision | Substantially Equivalent, Oct 13, 1994 |
| Received | Mar 22, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941351
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.