Clearance Summary
GLUCOSE DETERM. KIT received FDA 510(k) clearance under submission number K781307, sponsored by Analytical & Research Chemicals, 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 1978-08-31.
- Submission: K781307
- Applicant / Sponsor: Analytical & Research Chemicals, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1345
- Decision date: 1978-08-31
Classification & Regulation
This clearance is catalogued under FDA product code CGA and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.