syngo.CT View&GO
K-Number: K170952 · 2017-04-28
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2017-04-28
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
syngo.CT View&GO is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2017-04-28 under approval number K170952. 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.CT View&GO?
syngo.CT View&GO is a medical device that received FDA 510(k) clearance on 2017-04-28. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K170952.
When was syngo.CT View&GO approved by the FDA?
syngo.CT View&GO received FDA 510(k) clearance on 2017-04-28, under approval number K170952.
What company makes syngo.CT View&GO?
syngo.CT View&GO is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for syngo.CT View&GO?
The FDA product code for syngo.CT View&GO 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.