VARIVIEWER (X-RAY FILM VIEWER)— 510(k) K875233

Name: FDA 510(k) clearance K875233
Creator: U.S. Food and Drug Administration
Published: 1988-01-19

Substantially Equivalent

Diversified Diagnostic Products, Inc.

FDA 510(k) clearance K875233 for VARIVIEWER (X-RAY FILM VIEWER), Substantially Equivalent on 1988-01-19. Applicant: Diversified Diagnostic Products, Inc.. Device class: 1.

Clearance details

Applicant: Diversified Diagnostic Products, Inc.
Product code: Code IXC
Device class: Class 1
Regulation: 21 CFR 892.1890
Advisory panel: Radiology
Date received: 1987-12-22
Decision date: 1988-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

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K954998 — LILY DARK VIEWER1996-01-29

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