L/U ARM-VASCULAR— 510(k) K781571

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K781571 for L/U ARM-VASCULAR, Substantially Equivalent on 1978-11-27. Applicant: General Electric Co.. Device class: 1.

Clearance details

Applicant: General Electric Co.
Product code: Code IYB
Device class: Class 1
Regulation: 21 CFR 892.1770
Advisory panel: Radiology
Date received: 1978-09-14
Decision date: 1978-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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