meddevicedb.com FDA Device Reference

ECG & ULTRASOUND GELS, CREAMS & LOTION

K803151 Class II Traditional
Decision Date
1980-12-30
Sponsor / Applicant
Abco Dealers, Inc.

Technical Specification

510(k) Submission ID K803151
Product Code GYB
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1275
Decision Date 1980-12-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ECG & ULTRASOUND GELS, CREAMS & LOTION received FDA 510(k) clearance under submission number K803151, sponsored by Abco Dealers, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1980-12-30.

Classification & Regulation

This clearance is catalogued under FDA product code GYB and 21 CFR 882.1275, within the Neurology review panel as a Class II device.