Clearance Summary
AUTOMATED SLIDE SPINNER received FDA 510(k) clearance under submission number K771898, sponsored by Dynatech Cryomedical Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1977-10-18.
- Submission: K771898
- Applicant / Sponsor: Dynatech Cryomedical Co.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.5850
- Decision date: 1977-10-18
Classification & Regulation
This clearance is catalogued under FDA product code GKJ and 21 CFR 864.5850, within the Hematology review panel as a Class I device.