MULTIX Impact
K-Number: K193089 · 2020-03-20
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2020-03-20
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MULTIX Impact is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2020-03-20 under approval number K193089. 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 2020-03-20. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K193089.
When was MULTIX Impact approved by the FDA?
MULTIX Impact received FDA 510(k) clearance on 2020-03-20, under approval number K193089.
What company makes MULTIX Impact?
MULTIX Impact is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for MULTIX Impact?
The FDA product code for MULTIX Impact is KPR.
Other Devices by Siemens Medical Solutions USA, Inc.
Related Devices (Code: KPR)
K163203Carestream DRX-EvolutionCarestream Health, Inc.
K163115GC70Samsung Electronics Co., Ltd.
K152813FS-500DDR Medical Radiographic X-Ray SystemOrich Medical Equipment (Tianjin) Co., Ltd.
K162971Multix Fusion MaxSiemens Medical Solutions USA, Inc.
K161937CuattroDRCuattro, LLC
K162224ArtPix Mobile EZ2GOCmt Medical Technologies, Ltd.
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.