Clearance Summary
MODIFICATION TO ACIS (AUTOMATED CELLULAR IMAGING SYSTEM) received FDA 510(k) clearance under submission number K012138, sponsored by Chroma Vision Medical Systems, 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 2002-09-30.
- Submission: K012138
- Applicant / Sponsor: Chroma Vision Medical Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.1860
- Decision date: 2002-09-30
Classification & Regulation
This clearance is catalogued under FDA product code MYA and 21 CFR 864.1860, within the Hematology review panel as a Class II device.