Clearance Summary
SCOTT CM42 PASTEURIZER received FDA 510(k) clearance under submission number K810065, sponsored by William Harvey Life Products Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1981-01-28.
- Submission: K810065
- Applicant / Sponsor: William Harvey Life Products Corp.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5160
- Decision date: 1981-01-28
Classification & Regulation
This clearance is catalogued under FDA product code HGX and 21 CFR 884.5160, within the Obstetrics/Gynecology review panel as a Class II device.