510(k) K992930 ยท FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
BIOTEQUE HEMODIALYSIS BLOOD TUBING SET
| Applicant | Bioteque Corp., Flaggstaff AZ, US |
| Decision | Substantially Equivalent, Feb 9, 2000 |
| Received | Aug 31, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992930
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.