510(k) K960982 ยท FMI Needle, Hypodermic, Single Lumen
MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULA
| Applicant | Sherwood Medical Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Dec 23, 1996 |
| Received | Mar 11, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960982
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.