Clearance Summary
ANTI N DNA-HCP received FDA 510(k) clearance under submission number K830652, sponsored by Immuno-Products Industries. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1983-03-24.
- Submission: K830652
- Applicant / Sponsor: Immuno-Products Industries
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5100
- Decision date: 1983-03-24
Classification & Regulation
This clearance is catalogued under FDA product code KTL and 21 CFR 866.5100, within the Immunology review panel as a Class II device.