meddevicedb.com FDA Device Reference

Sterile Latex Powder Free Surgical Gloves

K253060 Class I Traditional
Decision Date
2026-05-22
Sponsor / Applicant
Protect Gloves Company Limited

Technical Specification

510(k) Submission ID K253060
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 2026-05-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sterile Latex Powder Free Surgical Gloves received FDA 510(k) clearance under submission number K253060, sponsored by Protect Gloves Company Limited. 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 2026-05-22.

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.