Clearance Summary
PROACTIVATOR C3, C4 AND C3 received FDA 510(k) clearance under submission number K790059, sponsored by Icl Scientific. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1979-03-15.
- Submission: K790059
- Applicant / Sponsor: Icl Scientific
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5260
- Decision date: 1979-03-15
Classification & Regulation
This clearance is catalogued under FDA product code KTP and 21 CFR 866.5260, within the Immunology review panel as a Class II device.