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FDA 510(k)

DIGITAL DIAGNOSTIC X-RAY SYSTEM MODEL XGEO GU60A

K-Number: K123106 · 2013-06-20

ApplicantSamsung Electronics Co., Ltd.
Decision Date2013-06-20
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL DIAGNOSTIC X-RAY SYSTEM MODEL XGEO GU60A is the device name listed in this FDA 510(k) record. The listed applicant is Samsung Electronics Co., Ltd.. It received FDA 510(k) clearance on 2013-06-20 under 510(k) number K123106. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL DIAGNOSTIC X-RAY SYSTEM MODEL XGEO GU60A?

DIGITAL DIAGNOSTIC X-RAY SYSTEM MODEL XGEO GU60A is a medical device that received FDA 510(k) clearance on 2013-06-20. The listed applicant is Samsung Electronics Co., Ltd.. The 510(k) number is K123106.

When did DIGITAL DIAGNOSTIC X-RAY SYSTEM MODEL XGEO GU60A receive FDA 510(k) clearance?

DIGITAL DIAGNOSTIC X-RAY SYSTEM MODEL XGEO GU60A received FDA 510(k) clearance on 2013-06-20, under 510(k) number K123106.

Who is the listed applicant for DIGITAL DIAGNOSTIC X-RAY SYSTEM MODEL XGEO GU60A?

The FDA 510(k) record lists Samsung Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL DIAGNOSTIC X-RAY SYSTEM MODEL XGEO GU60A?

The FDA product code for DIGITAL DIAGNOSTIC X-RAY SYSTEM MODEL XGEO GU60A is KPR.

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Other records listing Samsung Electronics Co., Ltd. as applicant

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Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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.

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