Clearance Summary
UROCUT BIOPSY NEEDLE received FDA 510(k) clearance under submission number K861267, sponsored by Meadox Surgimed, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1987-01-20.
- Submission: K861267
- Applicant / Sponsor: Meadox Surgimed, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1075
- Decision date: 1987-01-20
Classification & Regulation
This clearance is catalogued under FDA product code KNW and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.