Clearance Summary
AVL BLOOD GAS INSTRUMENT MODEL 939 received FDA 510(k) clearance under submission number K771147, sponsored by Jones Medical Instrument Co.. 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 1977-09-15.
- Submission: K771147
- Applicant / Sponsor: Jones Medical Instrument Co.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1120
- Decision date: 1977-09-15
Classification & Regulation
This clearance is catalogued under FDA product code CHL and 21 CFR 862.1120, within the Clinical Chemistry review panel as a Class II device.