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FDA 510(k)

MICRODELTA, GATED SINGLE PHOTON (SPECT) PACKAGE

K-Number: K900892 · 1990-05-02

ApplicantSiemens Gammasonics, Inc.
Decision Date1990-05-02
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MICRODELTA, GATED SINGLE PHOTON (SPECT) PACKAGE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Gammasonics, Inc.. It received FDA 510(k) clearance on 1990-05-02 under 510(k) number K900892. 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 MICRODELTA, GATED SINGLE PHOTON (SPECT) PACKAGE?

MICRODELTA, GATED SINGLE PHOTON (SPECT) PACKAGE is a medical device that received FDA 510(k) clearance on 1990-05-02. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K900892.

When did MICRODELTA, GATED SINGLE PHOTON (SPECT) PACKAGE receive FDA 510(k) clearance?

MICRODELTA, GATED SINGLE PHOTON (SPECT) PACKAGE received FDA 510(k) clearance on 1990-05-02, under 510(k) number K900892.

Who is the listed applicant for MICRODELTA, GATED SINGLE PHOTON (SPECT) PACKAGE?

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

What is the FDA product code for MICRODELTA, GATED SINGLE PHOTON (SPECT) PACKAGE?

The FDA product code for MICRODELTA, GATED SINGLE PHOTON (SPECT) PACKAGE is KPS.

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Other records listing Siemens Gammasonics, Inc. as applicant

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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

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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