510(k) K001233 ยท FPA Set, Administration, Intravascular
ACTI-FLEX FLUID DELIVERY SYSTEM OR ACTI-FLEX F D S
| Applicant | R-Group Intl., Gainesville FL, US |
| Decision | Substantially Equivalent, Dec 13, 2000 |
| Received | Apr 17, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001233
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.