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POWDERFREE GREEN LATEX EXAMINATION GLOVES (POLYMER COATED)

K980037 Class I Traditional
Decision Date
1998-02-09
Sponsor / Applicant
Sri Johani Sdn. Bhd.

Technical Specification

510(k) Submission ID K980037
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1998-02-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDERFREE GREEN LATEX EXAMINATION GLOVES (POLYMER COATED) received FDA 510(k) clearance under submission number K980037, sponsored by Sri Johani 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 1998-02-09.

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.