CARDIAC CATHETERIZATION LAB MONITOR SYS— 510(k) K770179

Name: FDA 510(k) clearance K770179
Creator: U.S. Food and Drug Administration
Published: 1977-04-05

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K770179 for CARDIAC CATHETERIZATION LAB MONITOR SYS, Substantially Equivalent on 1977-04-05. Applicant: General Electric Co.. Device class: 2.

Clearance details

Applicant: General Electric Co.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1977-01-27
Decision date: 1977-04-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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