510(k) K003123 ยท FIE Needle, Fistula
RENAX A.V. FISTULA NEEDLE SETS
| Applicant | Sunder Biomedical Tech. Co., Ltd., Taichung City, TW |
| Decision | Substantially Equivalent, May 4, 2001 |
| Received | Oct 5, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003123
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.