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MARK V DUPLEX ULTRASONIC SCANNING SYSTEM

K801598 Class II Traditional
Decision Date
1980-08-20
Sponsor / Applicant
Advanced Technology Laboratories, Inc.

Technical Specification

510(k) Submission ID K801598
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 1980-08-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MARK V DUPLEX ULTRASONIC SCANNING SYSTEM received FDA 510(k) clearance under submission number K801598, sponsored by Advanced Technology Laboratories, 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 1980-08-20.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.