Multix Fusion Max
K-Number: K162971 · 2016-11-22
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2016-11-22
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Multix Fusion Max is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2016-11-22 under approval number K162971. 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 Fusion Max?
Multix Fusion Max is a medical device that received FDA 510(k) clearance on 2016-11-22. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K162971.
When was Multix Fusion Max approved by the FDA?
Multix Fusion Max received FDA 510(k) clearance on 2016-11-22, under approval number K162971.
What company makes Multix Fusion Max?
Multix Fusion Max is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for Multix Fusion Max?
The FDA product code for Multix Fusion Max 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.