Clearance Summary
BOOTY ENDOSCOPE WARMER received FDA 510(k) clearance under submission number K933515, sponsored by T-Med, 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 1993-10-27.
- Submission: K933515
- Applicant / Sponsor: T-Med, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1993-10-27
Classification & Regulation
This clearance is catalogued under FDA product code GCI and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.