510(k) K934088 ยท FMI Needle, Hypodermic, Single Lumen
AUTO SUTURE SHARPS CONTAINER
| Applicant | United States Surgical, A Division of Tyco Healthc, Norwalk CT, US |
| Decision | Substantially Equivalent, Feb 3, 1994 |
| Received | Aug 24, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934088
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.