Clearance Summary
AUTOBEAD THYROID UPTAKE received FDA 510(k) clearance under submission number K930689, sponsored by Bio-Chem Laboratory Systems, 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 1993-11-10.
- Submission: K930689
- Applicant / Sponsor: Bio-Chem Laboratory Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2560
- Decision date: 1993-11-10
Classification & Regulation
This clearance is catalogued under FDA product code KHO and 21 CFR 862.2560, within the Clinical Chemistry review panel as a Class I device.