510(k) K153021 ยท DQA Oximeter
Fingertip Pulse Oximeter A310
| Applicant | Amemo, Inc., Milpitas CA, US |
| Decision | Substantially Equivalent, Nov 22, 2016 |
| Received | Oct 15, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153021
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.