ULTRASONIC PULSED DOPPLER IMAGING SYSTEM— 510(k) K903348

Name: FDA 510(k) clearance K903348
Creator: U.S. Food and Drug Administration
Published: 1990-10-22

Substantially Equivalent

Advanced Technology Laboratories, Inc.

FDA 510(k) clearance K903348 for ULTRASONIC PULSED DOPPLER IMAGING SYSTEM, Substantially Equivalent on 1990-10-22. Applicant: Advanced Technology Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Advanced Technology Laboratories, Inc.
Product code: Code HGL
Device class: Class 2
Regulation: 21 CFR 884.2960
Advisory panel: Obstetrics/Gynecology
Date received: 1990-07-26
Decision date: 1990-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

Download summary PDF View on FDA.gov ↗

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