510(k) K980062 ยท FMI Needle, Hypodermic, Single Lumen
MONOJECTT BLUNTIP I.V. ACCESS CANNULA WITH VIAL ACCESS PIN DEVICE
| Applicant | Davis & Geck, Inc., Hazlewood MO, US |
| Decision | Substantially Equivalent, Mar 20, 1998 |
| Received | Jan 7, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980062
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.