RMI ULTRASOUND DOPPLER PHANTOM SYSTEM— 510(k) K893216

Name: FDA 510(k) clearance K893216
Creator: U.S. Food and Drug Administration
Published: 1989-09-05

Substantially Equivalent

Radiation Measurements, Inc.

FDA 510(k) clearance K893216 for RMI ULTRASOUND DOPPLER PHANTOM SYSTEM, Substantially Equivalent on 1989-09-05. Applicant: Radiation Measurements, Inc.. Device class: 1.

Clearance details

Applicant: Radiation Measurements, Inc.
Product code: Code GXX
Device class: Class 1
Regulation: 21 CFR 882.1925
Advisory panel: Neurology
Date received: 1989-04-27
Decision date: 1989-09-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Middleton, WI, US

Download summary PDF View on FDA.gov ↗

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