Clearance Summary
LATEX POWDERED PATIENT EXAMINATION GLOVE, 200 MICROGRAMS OR LESS received FDA 510(k) clearance under submission number K011749, sponsored by Sempermed USA, 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 2001-08-22.
- Submission: K011749
- Applicant / Sponsor: Sempermed USA, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2001-08-22
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.