Symbia VA10A Family
K-Number: K210557 · 2021-05-12
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2021-05-12
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Symbia VA10A Family is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2021-05-12 under approval number K210557. 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 VA10A Family?
Symbia VA10A Family is a medical device that received FDA 510(k) clearance on 2021-05-12. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K210557.
When was Symbia VA10A Family approved by the FDA?
Symbia VA10A Family received FDA 510(k) clearance on 2021-05-12, under approval number K210557.
What company makes Symbia VA10A Family?
Symbia VA10A Family is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for Symbia VA10A Family?
The FDA product code for Symbia VA10A Family is KPS.
Other Devices by Siemens Medical Solutions USA, Inc.
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.