meddevicedb.com FDA Device Reference

POWERMAT VRP-1 X-RAY IMAGING

K840698 Class I Traditional
Decision Date
1984-03-16
Sponsor / Applicant
Powers Chemco, Inc.

Technical Specification

510(k) Submission ID K840698
Product Code IWZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1840
Decision Date 1984-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWERMAT VRP-1 X-RAY IMAGING received FDA 510(k) clearance under submission number K840698, sponsored by Powers Chemco, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1984-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code IWZ and 21 CFR 892.1840, within the Radiology review panel as a Class I device.