510(k) K210103 ยท FMF Syringe, Piston
SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX
| Applicant | Lifelong Meditech Private Limited, Gurgaon, IN |
| Decision | Substantially Equivalent, Jul 16, 2021 |
| Received | Jan 14, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210103
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.