DIRECT DIGITIZER, REGIUS MODEL 110— 510(k) K071181

Substantially Equivalent

Konica Minolta Medical & Graphic, Inc.

FDA 510(k) clearance K071181 for DIRECT DIGITIZER, REGIUS MODEL 110, Substantially Equivalent on 2007-05-30. Applicant: Konica Minolta Medical & Graphic, Inc..

Clearance details

Applicant: Konica Minolta Medical & Graphic, Inc.
Product code: Code MQB
Advisory panel: Radiology
Date received: 2007-04-30
Decision date: 2007-05-30
Decision: Substantially Equivalent
Clearance type: Special
Location: New York, NY, US

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