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FDA 510(k)

STV PRO 2

K-Number: K033419 · 2004-02-02

ApplicantTrophy Radiologie
Decision Date2004-02-02
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STV PRO 2 is the device name listed in this FDA 510(k) record. The listed applicant is Trophy Radiologie. It received FDA 510(k) clearance on 2004-02-02 under 510(k) number K033419. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STV PRO 2?

STV PRO 2 is a medical device that received FDA 510(k) clearance on 2004-02-02. The listed applicant is Trophy Radiologie. The 510(k) number is K033419.

When did STV PRO 2 receive FDA 510(k) clearance?

STV PRO 2 received FDA 510(k) clearance on 2004-02-02, under 510(k) number K033419.

Who is the listed applicant for STV PRO 2?

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

What is the FDA product code for STV PRO 2?

The FDA product code for STV PRO 2 is EIA.

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Related Devices (Code: EIA)

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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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