meddevicedb.com FDA Device Reference

NIL LATEX POWDERFREE EXAMINATION GLOVES

K955341 Class I Traditional
Decision Date
1996-04-26
Sponsor / Applicant
Shangrila Latex Industries Pvt. , Ltd.

Technical Specification

510(k) Submission ID K955341
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1996-04-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NIL LATEX POWDERFREE EXAMINATION GLOVES received FDA 510(k) clearance under submission number K955341, sponsored by Shangrila Latex Industries Pvt. , Ltd.. 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 1996-04-26.

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.