syngo.via MI Workflows
K-Number: K173897 · 2018-04-05
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2018-04-05
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
syngo.via MI Workflows is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2018-04-05 under approval number K173897. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the syngo.via MI Workflows?
syngo.via MI Workflows is a medical device that received FDA 510(k) clearance on 2018-04-05. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K173897.
When was syngo.via MI Workflows approved by the FDA?
syngo.via MI Workflows received FDA 510(k) clearance on 2018-04-05, under approval number K173897.
What company makes syngo.via MI Workflows?
syngo.via MI Workflows is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for syngo.via MI Workflows?
The FDA product code for syngo.via MI Workflows is LLZ.
Other Devices by Siemens Medical Solutions USA, Inc.
Related Devices (Code: LLZ)
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.