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FDA 510(k)

SCENIUM 1.1

K-Number: K061545 · 2006-06-30

ApplicantSiemens Molecular Imaging, Ltd.
Decision Date2006-06-30
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SCENIUM 1.1 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Molecular Imaging, Ltd.. It received FDA 510(k) clearance on 2006-06-30 under 510(k) number K061545. 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 SCENIUM 1.1?

SCENIUM 1.1 is a medical device that received FDA 510(k) clearance on 2006-06-30. The listed applicant is Siemens Molecular Imaging, Ltd.. The 510(k) number is K061545.

When did SCENIUM 1.1 receive FDA 510(k) clearance?

SCENIUM 1.1 received FDA 510(k) clearance on 2006-06-30, under 510(k) number K061545.

Who is the listed applicant for SCENIUM 1.1?

The FDA 510(k) record lists Siemens Molecular Imaging, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCENIUM 1.1?

The FDA product code for SCENIUM 1.1 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 Siemens Molecular Imaging, 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.

K042863SCENIUM

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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