510(k) K981386 ยท FPA Set, Administration, Intravascular
MANAN BLUNT NEEDLE
| Applicant | Manan Medical Products, Inc., Northbrook IL, US |
| Decision | Substantially Equivalent, Jun 29, 1998 |
| Received | Apr 16, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981386
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.