Clearance Summary
GEMENI IGM ASSAY received FDA 510(k) clearance under submission number K800450, sponsored by Electro-Nucleonics Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1980-04-24.
- Submission: K800450
- Applicant / Sponsor: Electro-Nucleonics Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5550
- Decision date: 1980-04-24
Classification & Regulation
This clearance is catalogued under FDA product code DAO and 21 CFR 866.5550, within the Immunology review panel as a Class II device.