meddevicedb.com FDA Device Reference

CHAMP-PAQ VINYL PATIENT EXAM GLOVES

K892098 Class I Traditional
Decision Date
1989-04-28
Sponsor / Applicant
Winmed Instruments Mfg. Corp.

Technical Specification

510(k) Submission ID K892098
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1989-04-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHAMP-PAQ VINYL PATIENT EXAM GLOVES received FDA 510(k) clearance under submission number K892098, sponsored by Winmed Instruments Mfg. Corp.. 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 1989-04-28.

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.