Clearance Summary
IN-VITRO DIAGNOSTIC REAGENT SET received FDA 510(k) clearance under submission number K930074, sponsored by Horizon Diagnostics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1993-05-11.
- Submission: K930074
- Applicant / Sponsor: Horizon Diagnostics, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1495
- Decision date: 1993-05-11
Classification & Regulation
This clearance is catalogued under FDA product code JGJ and 21 CFR 862.1495, within the Clinical Chemistry review panel as a Class I device.