REGIUS SIGMA2— 510(k) K120131

Substantially Equivalent

Konica Minolta Medical & Graphic, Inc.

FDA 510(k) clearance K120131 for REGIUS SIGMA2, Substantially Equivalent on 2012-02-10. Applicant: Konica Minolta Medical & Graphic, Inc..

Clearance details

Applicant: Konica Minolta Medical & Graphic, Inc.
Product code: Code MQB
Advisory panel: Radiology
Date received: 2012-01-17
Decision date: 2012-02-10
Decision: Substantially Equivalent
Clearance type: Special
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.