510(k) K013634 ยท FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK
| Applicant | Bioteque Corp., Flagstaff AZ, US |
| Decision | Unknown, Jul 9, 2002 |
| Received | Nov 5, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013634
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.