510(k) K111617 ยท DQA Oximeter
PULSE OXIMETER MODEL AB-F1/AH-S1/AH-M1
| Applicant | Acare Technology Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Dec 22, 2011 |
| Received | Jun 10, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111617
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.