Clearance Summary
INNOVATIVE GLOVES, LATEX EXAMINATION GLOVES POWDERFREE received FDA 510(k) clearance under submission number K993222, sponsored by Innovative Gloves Co;, Ltd.. 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 1999-11-05.
- Submission: K993222
- Applicant / Sponsor: Innovative Gloves Co;, Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 1999-11-05
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.