510(k) K831747 ยท FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
PLASMA THERAPY TUBESET-E100 SERIES
| Applicant | Parker Hannifin Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 30, 1983 |
| Received | Jun 1, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831747
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.