Clearance Summary
cobas m 511 integrated hematology analyzer received FDA 510(k) clearance under submission number K171655, sponsored by Roche Diagnostics Hematology, 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 2018-03-02.
- Submission: K171655
- Applicant / Sponsor: Roche Diagnostics Hematology, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5220
- Decision date: 2018-03-02
Classification & Regulation
This clearance is catalogued under FDA product code GKZ and 21 CFR 864.5220, within the Hematology review panel as a Class II device.