Clearance Summary
VANGUARD REPROCESSED NON-ELECTRIC BIOPSY FORCEPS received FDA 510(k) clearance under submission number K042594, sponsored by Vanguard Medical Concepts, 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 2005-01-25.
- Submission: K042594
- Applicant / Sponsor: Vanguard Medical Concepts, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.1075
- Decision date: 2005-01-25
Classification & Regulation
This clearance is catalogued under FDA product code NON and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class I device.