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FDA 510(k)

CIARTIC Move (VB10)

K-Number: K233748 · 2024-03-15

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2024-03-15
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CIARTIC Move (VB10) is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2024-03-15 under approval number K233748. 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 CIARTIC Move (VB10)?

CIARTIC Move (VB10) is a medical device that received FDA 510(k) clearance on 2024-03-15. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K233748.

When was CIARTIC Move (VB10) approved by the FDA?

CIARTIC Move (VB10) received FDA 510(k) clearance on 2024-03-15, under approval number K233748.

What company makes CIARTIC Move (VB10)?

CIARTIC Move (VB10) is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for CIARTIC Move (VB10)?

The FDA product code for CIARTIC Move (VB10) is OWB.

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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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