MULTIX Impact E
K-Number: K233532 · 2023-11-29
Device Summary
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. The listed applicant is Siemens Medical Solutions. The 510(k) number is K233532.
When did MULTIX Impact E receive FDA 510(k) clearance?
MULTIX Impact E received FDA 510(k) clearance on 2023-11-29, under 510(k) number K233532.
Who is the listed applicant for MULTIX Impact E?
The FDA 510(k) record lists Siemens Medical Solutions as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTIX Impact E?
The FDA product code for MULTIX Impact E is KPR.
Other records listing Siemens Medical Solutions 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.