510(k) K201726 ยท DQY Catheter, Percutaneous
Arterial Catheter
| Applicant | Haolang Medical USA Corporation, Bellevue WA, US |
| Decision | Substantially Equivalent, Jul 7, 2021 |
| Received | Jun 23, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201726
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.