Clearance Summary
SIGMA DIAGNOSTICS ALEXIN LS, MODELS A1219, A1334 received FDA 510(k) clearance under submission number K992712, sponsored by Sigma Diagnostics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1999-12-06.
- Submission: K992712
- Applicant / Sponsor: Sigma Diagnostics, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7925
- Decision date: 1999-12-06
Classification & Regulation
This clearance is catalogued under FDA product code GFO and 21 CFR 864.7925, within the Hematology review panel as a Class II device.