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FDA 510(k)

MODIFICATION TO WBR, MODEL HR

K-Number: K031874 · 2003-07-18

ApplicantU.C.G. Technologies , Ltd.
Decision Date2003-07-18
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO WBR, MODEL HR is the device name listed in this FDA 510(k) record. The listed applicant is U.C.G. Technologies , Ltd.. It received FDA 510(k) clearance on 2003-07-18 under 510(k) number K031874. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO WBR, MODEL HR?

MODIFICATION TO WBR, MODEL HR is a medical device that received FDA 510(k) clearance on 2003-07-18. The listed applicant is U.C.G. Technologies , Ltd.. The 510(k) number is K031874.

When did MODIFICATION TO WBR, MODEL HR receive FDA 510(k) clearance?

MODIFICATION TO WBR, MODEL HR received FDA 510(k) clearance on 2003-07-18, under 510(k) number K031874.

Who is the listed applicant for MODIFICATION TO WBR, MODEL HR?

The FDA 510(k) record lists U.C.G. Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO WBR, MODEL HR?

The FDA product code for MODIFICATION TO WBR, MODEL HR is KPS.

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.

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Other records listing U.C.G. Technologies , Ltd. 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.

K030870WBR, MODEL HR

Related Devices (Code: KPS)

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.

K261305MICSI-PETMicrostructure Imaging, Inc.K261427uMI Panvivo (uMI Panvivo M)Shanghai United Imaging Healthcare Co., Ltd.K261315Symbia Pro.specta Q3 (11364751);Symbia Pro.specta X3 (11364752);Symbia Pro.specta X7 (11364753);Symbia Pro.specta VA40 FamilySiemens Medical Solutions USA, Inc.K260524uMI Panvivo (uMI Panvivo LS); uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES)Shanghai United Imaging Healthcare Co., Ltd.K253564uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES)Shanghai United Imaging Healthcare Co., Ltd.K254001VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464)Spectrum Dynamics Medical, Ltd.

Official Source

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

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