KONICA DIRECT DIGITIZER REGIUS MODEL 350— 510(k) K013054

Substantially Equivalent

Konica Minolta Medical & Graphic, Inc.

FDA 510(k) clearance K013054 for KONICA DIRECT DIGITIZER REGIUS MODEL 350, Substantially Equivalent on 2002-03-01. Applicant: Konica Minolta Medical & Graphic, Inc..

Clearance details

Applicant: Konica Minolta Medical & Graphic, Inc.
Product code: Code MQB
Advisory panel: Radiology
Date received: 2001-09-11
Decision date: 2002-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hachioji-Shi Tokyo, JP

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