510(k) K001106 ยท FPA Set, Administration, Intravascular
MASTERSITE NEEDLELESS LUER ACTIVATED IV CONNECTOR, MODEL MS 1000
| Applicant | Creative Plastic Technology, Dana Point CA, US |
| Decision | Substantially Equivalent, Aug 16, 2000 |
| Received | Apr 5, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001106
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.