meddevicedb.com FDA Device Reference

POWDER-FREE, NATURAL COLOR, LATEX SURGICAL GLOVE, STERILE

K101102 Class I Traditional
Decision Date
2010-07-16
Sponsor / Applicant
Best Putra Gloves Sdn Bhd

Technical Specification

510(k) Submission ID K101102
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 2010-07-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWDER-FREE, NATURAL COLOR, LATEX SURGICAL GLOVE, STERILE received FDA 510(k) clearance under submission number K101102, sponsored by Best Putra Gloves 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 2010-07-16.

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.