Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

REGIUS SIGMA2

K-Number: K120131 · 2012-02-10

ApplicantKonica Minolta Medical & Graphic, Inc.
Decision Date2012-02-10
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

REGIUS SIGMA2 is the device name listed in this FDA 510(k) record. The listed applicant is Konica Minolta Medical & Graphic, Inc.. It received FDA 510(k) clearance on 2012-02-10 under 510(k) number K120131. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REGIUS SIGMA2?

REGIUS SIGMA2 is a medical device that received FDA 510(k) clearance on 2012-02-10. The listed applicant is Konica Minolta Medical & Graphic, Inc.. The 510(k) number is K120131.

When did REGIUS SIGMA2 receive FDA 510(k) clearance?

REGIUS SIGMA2 received FDA 510(k) clearance on 2012-02-10, under 510(k) number K120131.

Who is the listed applicant for REGIUS SIGMA2?

The FDA 510(k) record lists Konica Minolta Medical & Graphic, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REGIUS SIGMA2?

The FDA product code for REGIUS SIGMA2 is MQB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Konica Minolta Medical & Graphic, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K130936AERODR SYSTEM WITH P-31K123499AEROPILOTK120752AERODR STITCHING SYSTEMK121109AERODR X70K120477AEROSYNC FOR AERODR SYSTEMK113248AERODR SYSTEM WITH P-21

View all 27 devices →

Related Devices (Code: MQB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K2538000909FCE, 0909FCE-HSRayence Co., Ltd.K260820VIVIX-S 4386W (FXRD-4386WA)Vieworks Co., Ltd.K252996Universal 1417PIKonica Minolta Healthcare Americas, Inc.K252911Lux HD 2530 detector (Lux HD 2530)Iray Imaging Technology (Haining) LimitedK250211Yushan X-Ray Flat Panel DetectorInnocare Optoelectronics Corp.K250665SKR 3000Konica Minolta, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑