510(k) K001853 ยท FMI Needle, Hypodermic, Single Lumen
SYRINGE MANAGEMENT SYSTEM, MODEL SMS-1
| Applicant | Medtech Systems, Inc., Golden Valley MN, US |
| Decision | Substantially Equivalent, Aug 22, 2001 |
| Received | Jun 19, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001853
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.