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HIGH RISK POWDERED LATEX EXAMINATION GLOVES (BLUE COLOUR)

K973815 Class I Traditional
Decision Date
1997-11-21
Sponsor / Applicant
Sri Johani Sdn. Bhd.

Technical Specification

510(k) Submission ID K973815
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1997-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HIGH RISK POWDERED LATEX EXAMINATION GLOVES (BLUE COLOUR) received FDA 510(k) clearance under submission number K973815, 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 1997-11-21.

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.