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FDA 510(k)

STASYS MOTION CORRECTION SOFTWARE

K-Number: K082904 · 2008-12-17

ApplicantDigirad Corp.
Decision Date2008-12-17
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STASYS MOTION CORRECTION SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Digirad Corp.. It received FDA 510(k) clearance on 2008-12-17 under 510(k) number K082904. 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 STASYS MOTION CORRECTION SOFTWARE?

STASYS MOTION CORRECTION SOFTWARE is a medical device that received FDA 510(k) clearance on 2008-12-17. The listed applicant is Digirad Corp.. The 510(k) number is K082904.

When did STASYS MOTION CORRECTION SOFTWARE receive FDA 510(k) clearance?

STASYS MOTION CORRECTION SOFTWARE received FDA 510(k) clearance on 2008-12-17, under 510(k) number K082904.

Who is the listed applicant for STASYS MOTION CORRECTION SOFTWARE?

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

What is the FDA product code for STASYS MOTION CORRECTION SOFTWARE?

The FDA product code for STASYS MOTION CORRECTION SOFTWARE is KPS.

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Other records listing Digirad Corp. 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.

K123408ERGO IMAGING SYSTEMK100838ERGO IMAGING SYSTEMK083649CARDIUS 3 X-ACTK082368CARDIUS-1, -2, -3, AND CARDIUS 1,2,3 XPO SPECT IMAGING SYSTEMS, 2020TC SPECT IMAGING SYSTEMK070542CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMSK052430CARDIUS-1, CARDIUS-2, CARDIUS-3, 2020TC SPECT IMAGING SYSTEM

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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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