Viamo c100 TUS-VC100 Diagnostic Ultrasound System
K-Number: K173962 · 2018-04-20
ApplicantToshibamedical Systems Corporation
Decision Date2018-04-20
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Viamo c100 TUS-VC100 Diagnostic Ultrasound System is a medical device manufactured by Toshibamedical Systems Corporation. It received FDA 510(k) clearance on 2018-04-20 under approval number K173962. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Viamo c100 TUS-VC100 Diagnostic Ultrasound System?
Viamo c100 TUS-VC100 Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2018-04-20. It is manufactured by Toshibamedical Systems Corporation. The 510(k) number is K173962.
When was Viamo c100 TUS-VC100 Diagnostic Ultrasound System approved by the FDA?
Viamo c100 TUS-VC100 Diagnostic Ultrasound System received FDA 510(k) clearance on 2018-04-20, under approval number K173962.
What company makes Viamo c100 TUS-VC100 Diagnostic Ultrasound System?
Viamo c100 TUS-VC100 Diagnostic Ultrasound System is manufactured by Toshibamedical Systems Corporation.
What is the FDA product code for Viamo c100 TUS-VC100 Diagnostic Ultrasound System?
The FDA product code for Viamo c100 TUS-VC100 Diagnostic Ultrasound System is IYN.
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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.