510(k) K922179 ยท FMI Needle, Hypodermic, Single Lumen
CATHETER INSERTION TRAY
| Applicant | Medcare Custom Packaging, Inc., E Swanzey NH, US |
| Decision | Unknown, Jul 2, 1993 |
| Received | May 8, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922179
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.