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FDA 510(k)

Vereos PET/CT

K-Number: K210880 · 2021-05-19

ApplicantPhilips Medical Systems Nederland B.V.
Decision Date2021-05-19
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Vereos PET/CT is a medical device manufactured by Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2021-05-19 under approval number K210880. 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 Vereos PET/CT?

Vereos PET/CT is a medical device that received FDA 510(k) clearance on 2021-05-19. It is manufactured by Philips Medical Systems Nederland B.V.. The 510(k) number is K210880.

When was Vereos PET/CT approved by the FDA?

Vereos PET/CT received FDA 510(k) clearance on 2021-05-19, under approval number K210880.

What company makes Vereos PET/CT?

Vereos PET/CT is manufactured by Philips Medical Systems Nederland B.V..

What is the FDA product code for Vereos PET/CT?

The FDA product code for Vereos PET/CT is KPS.

Other Devices by Philips Medical Systems Nederland B.V.

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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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