Clearance Summary
MEDI, CURI EXAM GLOVES received FDA 510(k) clearance under submission number K893060, sponsored by Golden Charter , 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 1990-09-04.
- Submission: K893060
- Applicant / Sponsor: Golden Charter , Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 1990-09-04
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.