Clearance Summary
ANTI SERA TO HUMAN OROSCOMUCOID received FDA 510(k) clearance under submission number K823765, sponsored by Kent Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1982-12-30.
- Submission: K823765
- Applicant / Sponsor: Kent Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class I
- Regulation citation: 21 CFR 866.5420
- Decision date: 1982-12-30
Classification & Regulation
This clearance is catalogued under FDA product code DEX and 21 CFR 866.5420, within the Immunology review panel as a Class I device.