510(k) K222271 ยท FMI Needle, Hypodermic, Single Lumen
Verisafe Safety sterile needles
| Applicant | Promisemed Hangzhou Meditech Co., Ltd., Hangzhou City, CN |
| Decision | Substantially Equivalent, Feb 15, 2023 |
| Received | Jul 29, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222271
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.