Clearance Summary
AGEN DIMERTEST EIA received FDA 510(k) clearance under submission number K890189, sponsored by Agen Biomedical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1989-03-03.
- Submission: K890189
- Applicant / Sponsor: Agen Biomedical , Ltd.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7320
- Decision date: 1989-03-03
Classification & Regulation
This clearance is catalogued under FDA product code DAP and 21 CFR 864.7320, within the Hematology review panel as a Class II device.