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FDA 510(k)

ARTIS pheno (VE2)

K-Number: K201156 · 2020-06-29

ApplicantSiemens Medical Solution USA, Inc.
Decision Date2020-06-29
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARTIS pheno (VE2) is a medical device manufactured by Siemens Medical Solution USA, Inc.. It received FDA 510(k) clearance on 2020-06-29 under approval number K201156. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTIS pheno (VE2)?

ARTIS pheno (VE2) is a medical device that received FDA 510(k) clearance on 2020-06-29. It is manufactured by Siemens Medical Solution USA, Inc.. The 510(k) number is K201156.

When was ARTIS pheno (VE2) approved by the FDA?

ARTIS pheno (VE2) received FDA 510(k) clearance on 2020-06-29, under approval number K201156.

What company makes ARTIS pheno (VE2)?

ARTIS pheno (VE2) is manufactured by Siemens Medical Solution USA, Inc..

What is the FDA product code for ARTIS pheno (VE2)?

The FDA product code for ARTIS pheno (VE2) is OWB.

Other Devices by Siemens Medical Solution USA, Inc.

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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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