510(k) K052669 ยท DQA Oximeter
AVANT DIGITAL PULSE OXIMETRY SYSTEM, MODEL 4000, 4100
| Applicant | Nonin Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Dec 23, 2005 |
| Received | Sep 27, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052669
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.