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FDA 510(k)

Symbia Pro.specta VA20A Family

K-Number: K231102 · 2023-05-17

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2023-05-17
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Symbia Pro.specta VA20A Family is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2023-05-17 under approval number K231102. 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 Symbia Pro.specta VA20A Family?

Symbia Pro.specta VA20A Family is a medical device that received FDA 510(k) clearance on 2023-05-17. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K231102.

When was Symbia Pro.specta VA20A Family approved by the FDA?

Symbia Pro.specta VA20A Family received FDA 510(k) clearance on 2023-05-17, under approval number K231102.

What company makes Symbia Pro.specta VA20A Family?

Symbia Pro.specta VA20A Family is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for Symbia Pro.specta VA20A Family?

The FDA product code for Symbia Pro.specta VA20A Family is KPS.

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Related Devices (Code: KPS)

K161740D-SPECT Scanner, D-SPECT L ScannerSpectrum Dynamics Medical, Ltd. K162736Biograph Horizon PET/CT and Biograph mCT PET/CT and Biograph mCT Flow PET/CTSiemens Medical Solutions USA, Inc. K161674QuantumCamDdd-Diagnostic A/S K162337Symbia 6.5Siemens Medical Solutions USA, Inc. K161574Discovery MIGe Medical Systems, LLC K161631MAMMIGeneral Equipment For Medical Imaging

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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