Clearance Summary
VANGUARD REPROCESSED SUTURE PASSER received FDA 510(k) clearance under submission number K053585, sponsored by Ascent Healthcare Solutions. 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 2006-10-11.
- Submission: K053585
- Applicant / Sponsor: Ascent Healthcare Solutions
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2006-10-11
Classification & Regulation
This clearance is catalogued under FDA product code NLM and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.