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LYMPHA VISION-EXPERT

K003896 Class II Abbreviated
Decision Date
2002-04-24
Sponsor / Applicant
Bexley Trading, Inc.

Technical Specification

510(k) Submission ID K003896
Product Code GXY
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1320
Decision Date 2002-04-24
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LYMPHA VISION-EXPERT received FDA 510(k) clearance under submission number K003896, sponsored by Bexley Trading, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2002-04-24.

Classification & Regulation

This clearance is catalogued under FDA product code GXY and 21 CFR 882.1320, within the Neurology review panel as a Class II device.