510(k) K212668 ยท FBK Endoscopic Injection Needle, Gastroenterology-Urology
Sclerotherapy Needle
| Applicant | Zhejiang Chuangxiang Medical Technology Co., Ltd., Hangzhou, CN |
| Decision | Substantially Equivalent, Feb 23, 2022 |
| Received | Aug 23, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212668
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.