Clearance Summary
QUIK-TEMP received FDA 510(k) clearance under submission number K800666, sponsored by Liquid Crystal Products, 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 1980-05-08.
- Submission: K800666
- Applicant / Sponsor: Liquid Crystal Products, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5630
- Decision date: 1980-05-08
Classification & Regulation
This clearance is catalogued under FDA product code KPP and 21 CFR 876.5630, within the Gastroenterology, Urology review panel as a Class II device.