510(k) K983926 ยท FPA Set, Administration, Intravascular
MPS GRAVITY FLOW CONTROL SET
| Applicant | Critical Device Corp., Brea CA, US |
| Decision | Substantially Equivalent, Jan 20, 1999 |
| Received | Nov 5, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983926
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.