510(k) K242632 · FMI Needle, Hypodermic, Single Lumen
Verifine® Pen Needles
| Applicant | Promisemed Hangzhou Meditech Co., Ltd., Hangzhou City, CN |
| Decision | Substantially Equivalent, Sep 26, 2024 |
| Received | Sep 3, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K242632
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.