510(k) K240092 ยท DQA Oximeter
Pulse Oximeter (YM101, YM102, YM103, YM104, YM201, YM301, YM202, YM302, YM111, YM112, YM113, YM114, YM211, YM212, YM314, YM601, YM602, YM401, YM402, YM403, YM501, YM502, YM503 and YM504)
| Applicant | Shenzhen Yimi Life Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Oct 25, 2024 |
| Received | Jan 12, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240092
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.