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FDA 510(k)

MULTIX Impact E

K-Number: K220919 · 2022-05-17

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2022-05-17
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIX Impact E is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2022-05-17 under approval number K220919. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIX Impact E?

MULTIX Impact E is a medical device that received FDA 510(k) clearance on 2022-05-17. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K220919.

When was MULTIX Impact E approved by the FDA?

MULTIX Impact E received FDA 510(k) clearance on 2022-05-17, under approval number K220919.

What company makes MULTIX Impact E?

MULTIX Impact E is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for MULTIX Impact E?

The FDA product code for MULTIX Impact E is KPR.

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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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