meddevicedb.com FDA Device Reference

IMAGE PROCESSING SYS A3

K832505 Class I Traditional
Decision Date
1983-09-12
Sponsor / Applicant
Metronic, Inc.

Technical Specification

510(k) Submission ID K832505
Product Code IYX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1100
Decision Date 1983-09-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMAGE PROCESSING SYS A3 received FDA 510(k) clearance under submission number K832505, sponsored by Metronic, 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 1983-09-12.

Classification & Regulation

This clearance is catalogued under FDA product code IYX and 21 CFR 892.1100, within the Radiology review panel as a Class I device.