Clearance Summary
BLOOD GAS CALIBRATION STANDARD received FDA 510(k) clearance under submission number K900819, sponsored by Cryogenic Rare Gas Laboratories, 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 1990-04-25.
- Submission: K900819
- Applicant / Sponsor: Cryogenic Rare Gas Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1660
- Decision date: 1990-04-25
Classification & Regulation
This clearance is catalogued under FDA product code LCH and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.