meddevicedb.com FDA Device Reference

620CSR DISPLAY DRIVER

K932894 Class II Traditional
Decision Date
1994-06-20
Sponsor / Applicant
Vidco, Inc.

Technical Specification

510(k) Submission ID K932894
Product Code DXJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2450
Decision Date 1994-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

620CSR DISPLAY DRIVER received FDA 510(k) clearance under submission number K932894, sponsored by Vidco, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1994-06-20.

Classification & Regulation

This clearance is catalogued under FDA product code DXJ and 21 CFR 870.2450, within the Cardiovascular review panel as a Class II device.