510(k) K123801 ยท DQA Oximeter
FINGER PULSE OXIMETER
| Applicant | Shenzhen Kingyield Technology Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, May 28, 2013 |
| Received | Dec 10, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123801
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.