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CINE/VIEW PLUS - CARDIOLOGY WORKSTATION

K904977 Class II Traditional
Decision Date
1991-02-25
Sponsor / Applicant
Prism Imaging, Inc.

Technical Specification

510(k) Submission ID K904977
Product Code DXK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2330
Decision Date 1991-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CINE/VIEW PLUS - CARDIOLOGY WORKSTATION received FDA 510(k) clearance under submission number K904977, sponsored by Prism Imaging, 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 1991-02-25.

Classification & Regulation

This clearance is catalogued under FDA product code DXK and 21 CFR 870.2330, within the Cardiovascular review panel as a Class II device.