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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 the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2024-03-15 under 510(k) 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. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K233748.

When did CIARTIC Move (VB10) receive FDA 510(k) clearance?

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

Who is the listed applicant for CIARTIC Move (VB10)?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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