510(k) K010538 ยท FPA Set, Administration, Intravascular
PARSET NEEDLELESS PRIMARY SET FOR BLUNT CANNULA, A10003E, PARSET NEEDLELESS SECONDARY SET WITH BLUNT CANNULA, A14003E
| Applicant | Rd Medical Mfg., Inc., Cuelbra PR, US |
| Decision | Substantially Equivalent, Mar 30, 2001 |
| Received | Feb 23, 2001 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K010538
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.