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FDA 510(k)

RADspeed Pro

K-Number: K152244 · 2016-06-20

ApplicantShimadzu Corporation
Decision Date2016-06-20
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADspeed Pro is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Corporation. It received FDA 510(k) clearance on 2016-06-20 under 510(k) number K152244. 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 RADspeed Pro?

RADspeed Pro is a medical device that received FDA 510(k) clearance on 2016-06-20. The listed applicant is Shimadzu Corporation. The 510(k) number is K152244.

When did RADspeed Pro receive FDA 510(k) clearance?

RADspeed Pro received FDA 510(k) clearance on 2016-06-20, under 510(k) number K152244.

Who is the listed applicant for RADspeed Pro?

The FDA 510(k) record lists Shimadzu Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RADspeed Pro?

The FDA product code for RADspeed Pro is KPR.

Other records listing Shimadzu Corporation 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.

K252099TriniasK233719FDR Visionary SuiteK233722RADspeed ProK191877FLUOROspeedK190373SonialVision G4K173517RADspeed fit

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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.

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 HealthK252000uDR Arria & uDR ArisShanghai United Imaging Healthcare Co., Ltd.K251167uDR Aurora CXShanghai United Imaging Healthcare Co., Ltd.K250788Definium Tempo SelectGe Hualun Medical Systems Co. , Ltd.

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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