Clearance Summary
SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPER received FDA 510(k) clearance under submission number K882881, sponsored by Sakura Finetek U.S.A., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1988-07-28.
- Submission: K882881
- Applicant / Sponsor: Sakura Finetek U.S.A., Inc.
- Clearance pathway: Traditional
- Review panel: Pathology
- Device class: Class I
- Regulation citation: 21 CFR 864.3010
- Decision date: 1988-07-28
Classification & Regulation
This clearance is catalogued under FDA product code KES and 21 CFR 864.3010, within the Pathology review panel as a Class I device.