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FDA 510(k)

Sensis Vibe (VD15)

K-Number: K223812 · 2023-09-15

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2023-09-15
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Sensis Vibe (VD15) is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2023-09-15 under approval number K223812. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sensis Vibe (VD15)?

Sensis Vibe (VD15) is a medical device that received FDA 510(k) clearance on 2023-09-15. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K223812.

When was Sensis Vibe (VD15) approved by the FDA?

Sensis Vibe (VD15) received FDA 510(k) clearance on 2023-09-15, under approval number K223812.

What company makes Sensis Vibe (VD15)?

Sensis Vibe (VD15) is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for Sensis Vibe (VD15)?

The FDA product code for Sensis Vibe (VD15) is DQK.

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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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