Clearance Summary
DIAGNON B12 57CO RIA KIT received FDA 510(k) clearance under submission number K832717, sponsored by Diagnon Corp.. 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 1983-12-08.
- Submission: K832717
- Applicant / Sponsor: Diagnon Corp.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1810
- Decision date: 1983-12-08
Classification & Regulation
This clearance is catalogued under FDA product code CDD and 21 CFR 862.1810, within the Clinical Chemistry review panel as a Class II device.