510(k) K883764 ยท FPA Set, Administration, Intravascular
INTRAVASCULAR ADMINISTRATION SET
| Applicant | Device Labs, Inc., Medway MA, US |
| Decision | Substantially Equivalent, Dec 19, 1988 |
| Received | Sep 6, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883764
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.