510(k) K864310 ยท FMI Needle, Hypodermic, Single Lumen
RYMCO STERILE SINGLE-USE NEEDLE/SINGLE USE SYRINGE
| Applicant | Rymco Ltda, Coral Gables FL, US |
| Decision | Substantially Equivalent, Jan 20, 1987 |
| Received | Nov 3, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864310
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.