Vitrea Software Toshiba Package VSTP-001A
K-Number: K173088 · 2018-01-31
ApplicantToshibamedical Systems Corporation
Decision Date2018-01-31
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Vitrea Software Toshiba Package VSTP-001A is a medical device manufactured by Toshibamedical Systems Corporation. It received FDA 510(k) clearance on 2018-01-31 under approval number K173088. 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 Vitrea Software Toshiba Package VSTP-001A?
Vitrea Software Toshiba Package VSTP-001A is a medical device that received FDA 510(k) clearance on 2018-01-31. It is manufactured by Toshibamedical Systems Corporation. The 510(k) number is K173088.
When was Vitrea Software Toshiba Package VSTP-001A approved by the FDA?
Vitrea Software Toshiba Package VSTP-001A received FDA 510(k) clearance on 2018-01-31, under approval number K173088.
What company makes Vitrea Software Toshiba Package VSTP-001A?
Vitrea Software Toshiba Package VSTP-001A is manufactured by Toshibamedical Systems Corporation.
What is the FDA product code for Vitrea Software Toshiba Package VSTP-001A?
The FDA product code for Vitrea Software Toshiba Package VSTP-001A is LLZ.
Other Devices by Toshibamedical Systems Corporation
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.