510(k) K014140 ยท FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
RENAX HEMODIALYSIS BLOOD TUBING SET; SUNDER HEMODIALYSIS BLOOD TUBING SET
| Applicant | Sunder Biomedical Tech. Co., Ltd., Taichung City, TW |
| Decision | Substantially Equivalent, Nov 18, 2002 |
| Received | Dec 17, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014140
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.