Clearance Summary
CELL-DYN DIFF SCREEN, AUTO. & SEMI AUTO. LYTIC AG. received FDA 510(k) clearance under submission number K873348, sponsored by Abbott Diagnostics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1987-09-09.
- Submission: K873348
- Applicant / Sponsor: Abbott Diagnostics
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.8540
- Decision date: 1987-09-09
Classification & Regulation
This clearance is catalogued under FDA product code GGK and 21 CFR 864.8540, within the Hematology review panel as a Class I device.