ARTIUS SYSTEM— 510(k) K771151

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K771151 for ARTIUS SYSTEM, Substantially Equivalent on 1977-08-04. Applicant: General Electric Co.. Device class: 2.

Clearance details

Applicant: General Electric Co.
Product code: Code HGL
Device class: Class 2
Regulation: 21 CFR 884.2960
Advisory panel: Obstetrics/Gynecology
Date received: 1977-06-24
Decision date: 1977-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.