Clearance Summary
ACCUTECH ENDOLITE PROBE received FDA 510(k) clearance under submission number K061025, sponsored by Accutech Medical Technologies, 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 2006-05-31.
- Submission: K061025
- Applicant / Sponsor: Accutech Medical Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2006-05-31
Classification & Regulation
This clearance is catalogued under FDA product code FFS and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.