510(k) K173123 ยท DQA Oximeter
Pulse Oximeter
| Applicant | Shenzhen Imdk Medical Technology Co., Ltd., Guangming District, Shenzhen, CN |
| Decision | Substantially Equivalent, Aug 13, 2018 |
| Received | Sep 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173123
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.