meddevicedb.com FDA Device Reference

INDICATENS MODEL 4X4 SP ELECTRODE STIM. PATCHES

K891105 Class II Traditional
Decision Date
1989-05-25
Sponsor / Applicant
Acudata Software

Technical Specification

510(k) Submission ID K891105
Product Code GXY
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1320
Decision Date 1989-05-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INDICATENS MODEL 4X4 SP ELECTRODE STIM. PATCHES received FDA 510(k) clearance under submission number K891105, sponsored by Acudata Software. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1989-05-25.

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.