FDA 510(k)

V-TREND TARGET RF TEST

K-Number: K904105 · 1990-10-15

Decision Date1990-10-15

Product CodeDHR

Advisory CommitteeIM

DecisionSubstantially Equivalent

Device Summary

V-TREND TARGET RF TEST is the device name listed in this FDA 510(k) record. The listed applicant is Texas Immunology, Inc.. It received FDA 510(k) clearance on 1990-10-15 under 510(k) number K904105. The device is classified under product code DHR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-TREND TARGET RF TEST?

V-TREND TARGET RF TEST is a medical device that received FDA 510(k) clearance on 1990-10-15. The listed applicant is Texas Immunology, Inc.. The 510(k) number is K904105.

When did V-TREND TARGET RF TEST receive FDA 510(k) clearance?

V-TREND TARGET RF TEST received FDA 510(k) clearance on 1990-10-15, under 510(k) number K904105.

Who is the listed applicant for V-TREND TARGET RF TEST?

The FDA 510(k) record lists Texas Immunology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V-TREND TARGET RF TEST?

The FDA product code for V-TREND TARGET RF TEST is DHR.

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Related Devices (Code: DHR)

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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.