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Powder Free Latex Patient Examination Glove, Black Colored, Non-sterile, with Protein Content labeling Claim (Contains 50 ug per dm2 of glove or less of Total Water Extractable Protein)

K230573 Class I Traditional
Decision Date
2023-06-13
Sponsor / Applicant
Kossan International Sdn Bhd

Technical Specification

510(k) Submission ID K230573
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2023-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Powder Free Latex Patient Examination Glove, Black Colored, Non-sterile, with Protein Content labeling Claim (Contains 50 ug per dm2 of glove or less of Total Water Extractable Protein) received FDA 510(k) clearance under submission number K230573, sponsored by Kossan International 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 2023-06-13.

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.