meddevicedb.com FDA Device Reference

POLYCHLOROPRENE POWDER FREE SURGICAL GLOVE (GREEN)

K170152 Class I Traditional
Decision Date
2017-05-05
Sponsor / Applicant
Hartalega Sdn Bhd

Technical Specification

510(k) Submission ID K170152
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 2017-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POLYCHLOROPRENE POWDER FREE SURGICAL GLOVE (GREEN) received FDA 510(k) clearance under submission number K170152, sponsored by Hartalega Sdn Bhd. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2017-05-05.

Classification & Regulation

This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.