V.I. OCTOSON ULTRASONIC SYSTEM— 510(k) K760874

Name: FDA 510(k) clearance K760874
Creator: U.S. Food and Drug Administration
Published: 1976-12-16

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K760874 for V.I. OCTOSON ULTRASONIC SYSTEM, Substantially Equivalent on 1976-12-16. Applicant: General Electric Co.. Device class: 2.

Clearance details

Applicant: General Electric Co.
Product code: Code HEM
Device class: Class 2
Regulation: 21 CFR 884.2225
Advisory panel: Obstetrics/Gynecology
Date received: 1976-10-18
Decision date: 1976-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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