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FDA 510(k)

MULTIX Impact E

K-Number: K233532 · 2023-11-29

ApplicantSiemens Medical Solutions
Decision Date2023-11-29
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIX Impact E is a medical device manufactured by Siemens Medical Solutions. It received FDA 510(k) clearance on 2023-11-29 under approval number K233532. 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 2023-11-29. It is manufactured by Siemens Medical Solutions. The 510(k) number is K233532.

When was MULTIX Impact E approved by the FDA?

MULTIX Impact E received FDA 510(k) clearance on 2023-11-29, under approval number K233532.

What company makes MULTIX Impact E?

MULTIX Impact E is manufactured by Siemens Medical Solutions.

What is the FDA product code for MULTIX Impact E?

The FDA product code for MULTIX Impact E is KPR.

Other Devices by Siemens Medical Solutions

K221281Multitom Rax K212212Multitom Rax with True2scale Body Scan Option K231577MOBILETT Impact K233543YSIO X.pree K250738YSIO X.pree K250660LUMINOS Q.namix T; LUMINOS Q.namix R

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Related Devices (Code: 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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