Clearance Summary
REAGENTS FOR DETERM. CO2 IN HUMAN SERUM received FDA 510(k) clearance under submission number K800681, sponsored by Diagnostic Solutions, 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 1980-05-30.
- Submission: K800681
- Applicant / Sponsor: Diagnostic Solutions, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1160
- Decision date: 1980-05-30
Classification & Regulation
This clearance is catalogued under FDA product code KMS and 21 CFR 862.1160, within the Clinical Chemistry review panel as a Class II device.