meddevicedb.com FDA Device Reference

DISPOSABLE VINYL (PVC) EXAMINATION GLOVES

K893796 Class I Traditional
Decision Date
1989-09-12
Sponsor / Applicant
Anmei Plastic & Rubber Products Co. , Ltd.

Technical Specification

510(k) Submission ID K893796
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1989-09-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE VINYL (PVC) EXAMINATION GLOVES received FDA 510(k) clearance under submission number K893796, sponsored by Anmei Plastic & Rubber Products Co. , 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 1989-09-12.

Classification & Regulation

This clearance is catalogued under FDA product code LYZ and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.