EVOLUTION ULTRASONIC— 510(k) K894215

Name: FDA 510(k) clearance K894215
Creator: U.S. Food and Drug Administration
Published: 1990-04-16

Substantially Equivalent

Medical Industries America, Inc.

FDA 510(k) clearance K894215 for EVOLUTION ULTRASONIC, Substantially Equivalent on 1990-04-16. Applicant: Medical Industries America, Inc.. Device class: 1.

Clearance details

Applicant: Medical Industries America, Inc.
Product code: Code CCQ
Device class: Class 1
Regulation: 21 CFR 868.5640
Advisory panel: Anesthesiology
Date received: 1989-06-19
Decision date: 1990-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Des Moines, IA, US

Download summary PDF View on FDA.gov ↗

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