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LATEX EXAMINATION GLOVE POWDER FREE, WITH PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS TOTAL WATER SOLUBLE PROTEIN)

K992031 Class I Traditional
Decision Date
1999-07-12
Sponsor / Applicant
Shanghai Changzheng Latex Factory

Technical Specification

510(k) Submission ID K992031
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1999-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LATEX EXAMINATION GLOVE POWDER FREE, WITH PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS TOTAL WATER SOLUBLE PROTEIN) received FDA 510(k) clearance under submission number K992031, sponsored by Shanghai Changzheng Latex Factory. 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 1999-07-12.

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.