510(k) K931658 ยท FPA Set, Administration, Intravascular
IN-LINE BURETTE SET
| Applicant | Douglas Medical Products Corp., Mundelein IL, US |
| Decision | Substantially Equivalent, Dec 21, 1993 |
| Received | Apr 5, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931658
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.