510(k) K913329 ยท FMI Needle, Hypodermic, Single Lumen
V-ACCI-GUARD(TM) REUSABLE HOLDER
| Applicant | Medical Safety Products, Inc., Denver CO, US |
| Decision | Substantially Equivalent, Aug 23, 1991 |
| Received | Jul 25, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913329
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.