510(k) K241793 ยท KNW Instrument, Biopsy
Automatic Core Biopsy Instrument/ Semi-Automatic Core Biopsy Instrument/ Disposable Coaxial Biopsy Needle
| Applicant | Zhejiang Curaway Medical Technology Co., Ltd., Hangzhou, CN |
| Decision | Substantially Equivalent, Jan 24, 2025 |
| Received | Jun 21, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241793
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.