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PATIENT EXAMINATION GLOVES DUBBLE BUTTERFLY

K892685 Class I Traditional
Decision Date
1989-08-10
Sponsor / Applicant
China National Chemical Construction Corp.-Qingdao

Technical Specification

510(k) Submission ID K892685
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1989-08-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PATIENT EXAMINATION GLOVES DUBBLE BUTTERFLY received FDA 510(k) clearance under submission number K892685, sponsored by China National Chemical Construction Corp.-Qingdao. 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 1989-08-10.

Classification & Regulation

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