510(k) K960661 ยท FPA Set, Administration, Intravascular
MAXCESS NEEDLE FREE CONNECTOR (8200)
| Applicant | Solopak Medical Products, Inc., Libertyville IL, US |
| Decision | Substantially Equivalent, Mar 21, 1996 |
| Received | Feb 16, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960661
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.