Clearance Summary
FISHER DIAG. PRIME BLOOD GAS CONTROLS received FDA 510(k) clearance under submission number K792143, sponsored by Fisher Scientific Co., LLC. 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 1979-11-13.
- Submission: K792143
- Applicant / Sponsor: Fisher Scientific Co., LLC
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1660
- Decision date: 1979-11-13
Classification & Regulation
This clearance is catalogued under FDA product code JJS and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.