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NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS

K905248 Class II Traditional
Decision Date
1991-02-28
Sponsor / Applicant
Advanced Technology Laboratories, Inc.

Technical Specification

510(k) Submission ID K905248
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 1991-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS received FDA 510(k) clearance under submission number K905248, sponsored by Advanced Technology Laboratories, 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 1991-02-28.

Classification & Regulation

This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.