Clearance Summary
ALCATRON AND / OR MULTIPLE BRAND received FDA 510(k) clearance under submission number K112222, sponsored by Alcatron Gloves Factory. 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 2011-10-27.
- Submission: K112222
- Applicant / Sponsor: Alcatron Gloves Factory
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2011-10-27
Classification & Regulation
This clearance is catalogued under FDA product code LYZ and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.