Clearance Summary
SCHIFF REAGENT received FDA 510(k) clearance under submission number K883217, sponsored by Surgipath Medical Industries, 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 1988-08-05.
- Submission: K883217
- Applicant / Sponsor: Surgipath Medical Industries, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.1850
- Decision date: 1988-08-05
Classification & Regulation
This clearance is catalogued under FDA product code HZT and 21 CFR 864.1850, within the Hematology review panel as a Class I device.