Clearance Summary
DISPOSABLE, STERILE BIOPSY PUNCH received FDA 510(k) clearance under submission number K853104, sponsored by August C. Stiefel Research Institute, 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 1985-10-04.
- Submission: K853104
- Applicant / Sponsor: August C. Stiefel Research Institute, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1075
- Decision date: 1985-10-04
Classification & Regulation
This clearance is catalogued under FDA product code FCI and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.