HYPERPACS PACS AND TELERAFIOLOGY SYSTEM— 510(k) K950343

Name: FDA 510(k) clearance K950343
Creator: U.S. Food and Drug Administration
Published: 1995-04-12

Substantially Equivalent

Rogan Imaging Corp.

FDA 510(k) clearance K950343 for HYPERPACS PACS AND TELERAFIOLOGY SYSTEM, Substantially Equivalent on 1995-04-12. Applicant: Rogan Imaging Corp.. Device class: 1.

Clearance details

Applicant: Rogan Imaging Corp.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1995-01-27
Decision date: 1995-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waukesha, WI, US

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