AERODR SYSTEM 2— 510(k) K141271

Substantially Equivalent

Konica Minolta, Inc.

FDA 510(k) clearance K141271 for AERODR SYSTEM 2, Substantially Equivalent on 2014-09-26. Applicant: Konica Minolta, Inc..

Clearance details

Applicant: Konica Minolta, Inc.
Product code: Code MQB
Advisory panel: Radiology
Date received: 2014-05-15
Decision date: 2014-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

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