Clearance Summary
T3 UPTAKE-SQUIBB DIAGNOSTIC KIT received FDA 510(k) clearance under submission number K820340, sponsored by E. R. Squibb & Sons, Inc.. 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 1982-03-04.
- Submission: K820340
- Applicant / Sponsor: E. R. Squibb & Sons, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1715
- Decision date: 1982-03-04
Classification & Regulation
This clearance is catalogued under FDA product code KHQ and 21 CFR 862.1715, within the Clinical Chemistry review panel as a Class II device.