Clearance Summary
DIAGNON FERRITIN 125 I RIA KIT received FDA 510(k) clearance under submission number K830580, sponsored by Iagnon Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1983-05-05.
- Submission: K830580
- Applicant / Sponsor: Iagnon Corp.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5340
- Decision date: 1983-05-05
Classification & Regulation
This clearance is catalogued under FDA product code DBF and 21 CFR 866.5340, within the Immunology review panel as a Class II device.