SKR 3000— 510(k) K241319

Substantially Equivalent

Konica Minolta, Inc.

FDA 510(k) clearance K241319 for SKR 3000, Substantially Equivalent on 2024-11-21. Applicant: Konica Minolta, Inc..

Clearance details

Applicant: Konica Minolta, Inc.
Product code: Code MQB
Advisory panel: Radiology
Date received: 2024-05-10
Decision date: 2024-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tokyo, JP

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