MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING— 510(k) K953477

Name: FDA 510(k) clearance K953477
Creator: U.S. Food and Drug Administration
Published: 1995-10-07

Substantially Equivalent

The DU Pont Co.

FDA 510(k) clearance K953477 for MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING, Substantially Equivalent on 1995-10-07. Applicant: The DU Pont Co.. Device class: 2.

Clearance details

Applicant: The DU Pont Co.
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 1995-07-24
Decision date: 1995-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilmington, DE, US

Download summary PDF View on FDA.gov ↗

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