meddevicedb.com FDA Device Reference

STERLING STYLE 90 SURGICAL GLOVES

K896675 Class I Traditional
Decision Date
1990-03-08
Sponsor / Applicant
Steril Rubber Sdn. Bhd.

Technical Specification

510(k) Submission ID K896675
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1990-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERLING STYLE 90 SURGICAL GLOVES received FDA 510(k) clearance under submission number K896675, sponsored by Steril Rubber 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 1990-03-08.

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.