Clearance Summary
AVL MODEL 912 CO-OXYLITE received FDA 510(k) clearance under submission number K895466, sponsored by Avl Scientific Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1989-11-06.
- Submission: K895466
- Applicant / Sponsor: Avl Scientific Corp.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7500
- Decision date: 1989-11-06
Classification & Regulation
This clearance is catalogued under FDA product code GLY and 21 CFR 864.7500, within the Hematology review panel as a Class II device.