510(k) K953823 ยท FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
ARTERIAL VENOUS BLOOD TUBING SET
| Applicant | Medisystems Corp., Washington DC, US |
| Decision | Substantially Equivalent, Sep 23, 1996 |
| Received | Aug 15, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953823
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.