Clearance Summary
GAMMA STIK 125I T3 UPTAKE KIT received FDA 510(k) clearance under submission number K780492, sponsored by Alpha Gamma Laboratory. 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 1978-04-28.
- Submission: K780492
- Applicant / Sponsor: Alpha Gamma Laboratory
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1710
- Decision date: 1978-04-28
Classification & Regulation
This clearance is catalogued under FDA product code CDP and 21 CFR 862.1710, within the Clinical Chemistry review panel as a Class II device.