510(k) K100020 ยท DQA Oximeter
DX SERIES FINGER SENSOR
| Applicant | Dixtal Medical, Inc., Wallingford CT, US |
| Decision | Substantially Equivalent, Mar 8, 2010 |
| Received | Jan 5, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K100020
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.