DIGITAL PRINTER P6000D SERIES, MODEL P6000DU— 510(k) K061302

Name: FDA 510(k) clearance K061302
Creator: U.S. Food and Drug Administration
Published: 2006-06-23

Substantially Equivalent

Mitsubishi Electric Corporation Kyoto Works

FDA 510(k) clearance K061302 for DIGITAL PRINTER P6000D SERIES, MODEL P6000DU, Substantially Equivalent on 2006-06-23. Applicant: Mitsubishi Electric Corporation Kyoto Works. Device class: 2.

Clearance details

Applicant: Mitsubishi Electric Corporation Kyoto Works
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 2006-05-10
Decision date: 2006-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ise-Shi, JP

Download summary PDF View on FDA.gov ↗

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