meddevicedb.com FDA Device Reference

CRW-1 SYSTEM

K944463 Class II Traditional
Decision Date
1995-10-26
Sponsor / Applicant
Radionics Software Applications, Inc.

Technical Specification

510(k) Submission ID K944463
Product Code HAW
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 1995-10-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CRW-1 SYSTEM received FDA 510(k) clearance under submission number K944463, sponsored by Radionics Software Applications, 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 1995-10-26.

Classification & Regulation

This clearance is catalogued under FDA product code HAW and 21 CFR 882.4560, within the Neurology review panel as a Class II device.