Clearance Summary
NEW FUCHSIN SOLUTION received FDA 510(k) clearance under submission number K871545, 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 1987-04-29.
- Submission: K871545
- Applicant / Sponsor: Sigma Diagnostics, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.1850
- Decision date: 1987-04-29
Classification & Regulation
This clearance is catalogued under FDA product code IDF and 21 CFR 864.1850, within the Hematology review panel as a Class I device.