510(k) K942179 ยท FMI Needle, Hypodermic, Single Lumen
PRO-TEC DISPOSABLE SHARPS CONTAINERS
| Applicant | Pro-Tec Containers, Inc., Lake Mary FL, US |
| Decision | Substantially Equivalent, Dec 2, 1994 |
| Received | May 4, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942179
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.