Clearance Summary
CYTOTECH C1-INHIBITOR ENZYME IMMUNOASSAY received FDA 510(k) clearance under submission number K872426, sponsored by Cytotech, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1987-07-23.
- Submission: K872426
- Applicant / Sponsor: Cytotech, Inc.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5250
- Decision date: 1987-07-23
Classification & Regulation
This clearance is catalogued under FDA product code DBA and 21 CFR 866.5250, within the Immunology review panel as a Class II device.