Clearance Summary
QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q received FDA 510(k) clearance under submission number K903641, sponsored by Bentley Laboratories, 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 1990-11-09.
- Submission: K903641
- Applicant / Sponsor: Bentley Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5860
- Decision date: 1990-11-09
Classification & Regulation
This clearance is catalogued under FDA product code KDI and 21 CFR 876.5860, within the Gastroenterology, Urology review panel as a Class II device.