510(k) K260517
K260517 is an FDA 510(k) premarket notification submitted by Zhejiang Curaway Medical Technology Co., Ltd. for the device "Automatic Core Biopsy Instrument". The FDA issued a decision of Substantially Equivalent on August 28, 2026. The device falls under product code KNW (Instrument, Biopsy), a Class II device regulated under 21 CFR 876.1075. Zhejiang Curaway Medical Technology Co., Ltd. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 28, 2026
- Date Received
- February 17, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Instrument, Biopsy
- Device Class
- Class II
- Regulation Number
- 876.1075
- Review Panel
- SU
- Submission Type