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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Toshibamedical Systems Corporation. It received FDA 510(k) clearance on 2018-01-31 under 510(k) 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. The listed applicant is Toshibamedical Systems Corporation. The 510(k) number is K173088.

When did Vitrea Software Toshiba Package VSTP-001A receive FDA 510(k) clearance?

Vitrea Software Toshiba Package VSTP-001A received FDA 510(k) clearance on 2018-01-31, under 510(k) number K173088.

Who is the listed applicant for Vitrea Software Toshiba Package VSTP-001A?

The FDA 510(k) record lists Toshibamedical Systems Corporation as the applicant. This does not by itself establish the device manufacturer.

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 records listing Toshibamedical Systems Corporation as applicant

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Related Devices (Code: LLZ)

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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.

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