Clearance Summary
ENSURE POWDER-FREE LATEX PATIENT EXAMINATION GLOVES received FDA 510(k) clearance under submission number K942643, sponsored by Basic Intl., 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 1994-10-07.
- Submission: K942643
- Applicant / Sponsor: Basic Intl., Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 1994-10-07
Classification & Regulation
This clearance is catalogued under FDA product code LYY and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.