510(k) K954267 ยท DQA Oximeter
BURDICK 200 PULSE OXIMETER
| Applicant | Burdick, Inc., Miltoon WI, US |
| Decision | Substantially Equivalent, May 3, 1996 |
| Received | Sep 12, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954267
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.