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UNIVISION ECHOCARDIOLOGY SYSTEM

K964803 Class I Traditional
Decision Date
1997-02-11
Sponsor / Applicant
Network Concepts, Inc.

Technical Specification

510(k) Submission ID K964803
Product Code LMB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2010
Decision Date 1997-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNIVISION ECHOCARDIOLOGY SYSTEM received FDA 510(k) clearance under submission number K964803, sponsored by Network Concepts, 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 1997-02-11.

Classification & Regulation

This clearance is catalogued under FDA product code LMB and 21 CFR 892.2010, within the Radiology review panel as a Class I device.