Clearance Summary
PATIENT EXAMINATION GLOVE received FDA 510(k) clearance under submission number K933602, sponsored by Kerala Rubber & Reclaims, 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 1995-01-02.
- Submission: K933602
- Applicant / Sponsor: Kerala Rubber & Reclaims, Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 1995-01-02
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.