510(k) K883638 ยท FPA Set, Administration, Intravascular
SAFESITE INJECTION SITE AND BLUNT CANNULA
| Applicant | Baxter Healthcare Corp, Round Lake IL, US |
| Decision | Substantially Equivalent, Sep 23, 1988 |
| Received | Aug 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883638
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.