Clearance Summary
BRAHMS DIAGNOSTICA DYNOTEST TG-PLUS received FDA 510(k) clearance under submission number K021057, sponsored by Brahms Diagnostica, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2002-09-17.
- Submission: K021057
- Applicant / Sponsor: Brahms Diagnostica, LLC
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.6010
- Decision date: 2002-09-17
Classification & Regulation
This clearance is catalogued under FDA product code MSW and 21 CFR 866.6010, within the Immunology review panel as a Class II device.