Clearance Summary
MODEL 7620 LINE CLAMP received FDA 510(k) clearance under submission number K792277, sponsored by B-D Drake Willock. 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 1980-01-16.
- Submission: K792277
- Applicant / Sponsor: B-D Drake Willock
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 1980-01-16
Classification & Regulation
This clearance is catalogued under FDA product code KOC and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.