Multix Fusion Max
K-Number: K162971 · 2016-11-22
Device Summary
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. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K162971.
When did Multix Fusion Max receive FDA 510(k) clearance?
Multix Fusion Max received FDA 510(k) clearance on 2016-11-22, under 510(k) number K162971.
Who is the listed applicant for Multix Fusion Max?
The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Multix Fusion Max?
The FDA product code for Multix Fusion Max is KPR.
Other records listing Siemens Medical Solutions USA, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KPR)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.