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FDA 510(k)

MULTIX Impact

K-Number: K182517 · 2019-01-11

ApplicantSiemens Medi Cal Solutions, Inc.
Decision Date2019-01-11
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIX Impact is a medical device manufactured by Siemens Medi Cal Solutions, Inc.. It received FDA 510(k) clearance on 2019-01-11 under approval number K182517. 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?

MULTIX Impact is a medical device that received FDA 510(k) clearance on 2019-01-11. It is manufactured by Siemens Medi Cal Solutions, Inc.. The 510(k) number is K182517.

When was MULTIX Impact approved by the FDA?

MULTIX Impact received FDA 510(k) clearance on 2019-01-11, under approval number K182517.

What company makes MULTIX Impact?

MULTIX Impact is manufactured by Siemens Medi Cal Solutions, Inc..

What is the FDA product code for MULTIX Impact?

The FDA product code for MULTIX Impact 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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