Clearance Summary
INSTANT-VIEW FECAL OCCULT BLOOD RAPID TEST received FDA 510(k) clearance under submission number K021423, sponsored by Alfa Scientific Designs, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2002-06-17.
- Submission: K021423
- Applicant / Sponsor: Alfa Scientific Designs, Inc.
- Clearance pathway: Abbreviated
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.6550
- Decision date: 2002-06-17
Classification & Regulation
This clearance is catalogued under FDA product code KHE and 21 CFR 864.6550, within the Hematology review panel as a Class II device.