REGIUS MODEL 170 DIRECT DIGITIZER— 510(k) K051998

Substantially Equivalent

Konica Minolta Medical & Graphic, Inc.

FDA 510(k) clearance K051998 for REGIUS MODEL 170 DIRECT DIGITIZER, Substantially Equivalent on 2005-11-03. Applicant: Konica Minolta Medical & Graphic, Inc..

Clearance details

Applicant: Konica Minolta Medical & Graphic, Inc.
Product code: Code MQB
Advisory panel: Radiology
Date received: 2005-07-25
Decision date: 2005-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hachioji-Shi, JP

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