510(k) K260517 ยท KNW Instrument, Biopsy
Automatic Core Biopsy Instrument
| Applicant | Zhejiang Curaway Medical Technology Co., Ltd., Hangzhou, CN |
| Decision | Substantially Equivalent, Aug 28, 2026 |
| Received | Feb 17, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260517
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.