Clearance Summary
MODULAR BIOPSY FORCEP received FDA 510(k) clearance under submission number K946360, sponsored by Cox Medical Ent., 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 1995-03-06.
- Submission: K946360
- Applicant / Sponsor: Cox Medical Ent., Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.1075
- Decision date: 1995-03-06
Classification & Regulation
This clearance is catalogued under FDA product code FCL and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class I device.