RAYTEL DIGITAL IMAGING SYSTEMS— 510(k) K922164

Name: FDA 510(k) clearance K922164
Creator: U.S. Food and Drug Administration
Published: 1993-01-21

Substantially Equivalent

Olicon Imaging Systems, Inc.

FDA 510(k) clearance K922164 for RAYTEL DIGITAL IMAGING SYSTEMS, Substantially Equivalent on 1993-01-21. Applicant: Olicon Imaging Systems, Inc.. Device class: 1.

Clearance details

Applicant: Olicon Imaging Systems, Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1992-05-08
Decision date: 1993-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Clemente, CA, US

Download summary PDF View on FDA.gov ↗

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