510(k) K914048 ยท FPA Set, Administration, Intravascular
NEEDLE*LOCK(TM) WITH INTERLINK(TM) INJECTION SITE
| Applicant | Baxter Healthcare Corp, Round Lake IL, US |
| Decision | Substantially Equivalent, Nov 27, 1991 |
| Received | Sep 10, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914048
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.