Clearance Summary
COAMATE(R) ANTITHROMBIN CHROMOGENIC ASSAY received FDA 510(k) clearance under submission number K915083, sponsored by Kabi Pharmacia, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1992-01-03.
- Submission: K915083
- Applicant / Sponsor: Kabi Pharmacia, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7060
- Decision date: 1992-01-03
Classification & Regulation
This clearance is catalogued under FDA product code JBQ and 21 CFR 864.7060, within the Hematology review panel as a Class II device.