REGUIS SIGMA— 510(k) K103703

Substantially Equivalent

Konica Minolta Medical & Graphic, Inc.

FDA 510(k) clearance K103703 for REGUIS SIGMA, Substantially Equivalent on 2011-06-02. Applicant: Konica Minolta Medical & Graphic, Inc..

Clearance details

Applicant: Konica Minolta Medical & Graphic, Inc.
Product code: Code MQB
Advisory panel: Radiology
Date received: 2010-12-20
Decision date: 2011-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

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