Clearance Summary
PATIENT EXAMINATION GLOVES (LATEX) received FDA 510(k) clearance under submission number K891630, sponsored by Inter-Continental Industries Sdn Bhd. 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 1989-05-11.
- Submission: K891630
- Applicant / Sponsor: Inter-Continental Industries Sdn Bhd
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 1989-05-11
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.