510(k) K952316 ยท DQA Oximeter
NELLCOR SYMPHONY N-3000 PULSE OXIMETER
| Applicant | Nellcor, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Aug 17, 1995 |
| Received | May 17, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952316
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.