510(k) K992626 ยท FMI Needle, Hypodermic, Single Lumen
SURE-WAY REUSABLE SHARPS CONTAINER
| Applicant | Sure-Way Systems, Inc., Wilmington CA, US |
| Decision | Substantially Equivalent, Dec 16, 1999 |
| Received | Aug 5, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992626
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.