Clearance Summary
ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III received FDA 510(k) clearance under submission number K931907, sponsored by Anthos Labtec Instruments. 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 1993-09-29.
- Submission: K931907
- Applicant / Sponsor: Anthos Labtec Instruments
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2300
- Decision date: 1993-09-29
Classification & Regulation
This clearance is catalogued under FDA product code JJQ and 21 CFR 862.2300, within the Clinical Chemistry review panel as a Class I device.