510(k) K032831 ยท DQA Oximeter
PRO 2 MONITOR, PRO 2 SENSOR, PRO2 HOLDER, PRO2 NEONATE HOLDER, MODELS, PRO- 200, ANS-200, AHL-200, NHL-200
| Applicant | Conmed Corporation, Utica NY, US |
| Decision | Substantially Equivalent, Aug 31, 2004 |
| Received | Sep 11, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032831
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.