Clearance Summary
DIMERTEST LATEX ASSAY received FDA 510(k) clearance under submission number K974596, 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 1998-05-26.
- Submission: K974596
- Applicant / Sponsor: Agen Biomedical , Ltd.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7320
- Decision date: 1998-05-26
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.