meddevicedb.com FDA Device Reference

ADVANTAGE

K885246 Class II Traditional
Decision Date
1989-02-27
Sponsor / Applicant
Clark Davis Medical Systems, Inc.

Technical Specification

510(k) Submission ID K885246
Product Code GWF
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1870
Decision Date 1989-02-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANTAGE received FDA 510(k) clearance under submission number K885246, sponsored by Clark Davis Medical Systems, 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 1989-02-27.

Classification & Regulation

This clearance is catalogued under FDA product code GWF and 21 CFR 882.1870, within the Neurology review panel as a Class II device.