Cleared Traditional

K890041 - V-TREND TARGET IM TEST

K890041 is the FDA 510(k) clearance for V-TREND TARGET IM TEST by Texas Immunology, Inc.. It is a Class 2 Immunology device (product code KTN) cleared through the Traditional 510(k) pathway after a 18-day FDA review.

K890041 · Texas Immunology, Inc. · Immunology device
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Jan 1989
Decision
18d
Days
Class 2
Risk

K890041 is an FDA 510(k) clearance for the V-TREND TARGET IM TEST. Classified as System, Test, Infectious Mononucleosis (product code KTN), Class II - Special Controls.

Submitted by Texas Immunology, Inc. (Tyler, US). The FDA issued a Cleared decision on January 23, 1989 after a review of 18 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5640 - the FDA immunology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Texas Immunology, Inc. devices

Submission Details

510(k) Number K890041 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 05, 1989
Decision Date January 23, 1989
Days to Decision 18 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
86d faster than avg
Panel avg: 104d · This submission: 18d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KTN System, Test, Infectious Mononucleosis
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5640
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Immunology devices follow this clearance model.

Regulatory Peers - KTN System, Test, Infectious Mononucleosis

All 26
Devices cleared under the same product code (KTN) and FDA review panel - the closest regulatory comparables to K890041.
DETECTADOT SYSTEM 2000 HETEROPHILE TEST
K895891 · Gull Laboratories, Inc. · Oct 1989
DIRECTIGEN 1-2-3 INFECTIOUS MONONUCLEOSIS TEST
K893737 · Quidel Corp. · Jun 1989
MONO-CUBE(TM)
K890991 · Difco Laboratories, Inc. · Mar 1989
MODIFICATION OF MONO-PLUS(TM)
K883709 · Armkel, LLC · Dec 1988
OXOID INFECTIOUS MONONUCLEOSIS KIT
K883540 · Unipath , Ltd. · Oct 1988
DIFFERENTIAL I.M. SCREENING TEST
K873297 · Sclavo, Inc. · Dec 1987