SONY DIGITAL PRINTER UP-D898MD/SONY HYBRID PRINTER UP-X898MD— 510(k) K141454

Name: FDA 510(k) clearance K141454
Creator: U.S. Food and Drug Administration
Published: 2014-06-26

Substantially Equivalent

Sony Electronics, Inc.

FDA 510(k) clearance K141454 for SONY DIGITAL PRINTER UP-D898MD/SONY HYBRID PRINTER UP-X898MD, Substantially Equivalent on 2014-06-26. 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: 2014-06-02
Decision date: 2014-06-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marlborough, MA, US

Download summary PDF View on FDA.gov ↗

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