SONY UP-DF750 DIGITAL FILM IMAGER— 510(k) K083522

Name: FDA 510(k) clearance K083522
Creator: U.S. Food and Drug Administration
Published: 2009-01-09

Substantially Equivalent

Sony Electronics, Inc.

FDA 510(k) clearance K083522 for SONY UP-DF750 DIGITAL FILM IMAGER, Substantially Equivalent on 2009-01-09. Applicant: Sony Electronics, Inc.. Device class: 2.

Clearance details

Applicant: Sony Electronics, Inc.
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 2008-11-26
Decision date: 2009-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleboro, MA, US

Download summary PDF View on FDA.gov ↗

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