Clearance Summary
SANA-LUBE received FDA 510(k) clearance under submission number K853653, sponsored by Huntington Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1985-11-13.
- Submission: K853653
- Applicant / Sponsor: Huntington Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6375
- Decision date: 1985-11-13
Classification & Regulation
This clearance is catalogued under FDA product code KMJ and 21 CFR 880.6375, within the General Hospital review panel as a Class I device.