Cleared Traditional

TRUST RPR TITRATION CARD TEST #65145

K832480 · Emd Chemicals, Inc. · Hematology
Sep 1983
Decision
48d
Days
Class 2
Risk

About This 510(k) Submission

K832480 is an FDA 510(k) clearance for the TRUST RPR TITRATION CARD TEST #65145, a Antigens, Nontreponemal, All (Class II — Special Controls, product code GMQ), submitted by Emd Chemicals, Inc. (Mchenry, US). The FDA issued a Cleared decision on September 12, 1983, 48 days after receiving the submission on July 26, 1983. This device falls under the Hematology review panel. Regulated under 21 CFR 866.3820.

Submission Details

510(k) Number K832480 FDA.gov
FDA Decision Cleared SESE
Date Received July 26, 1983
Decision Date September 12, 1983
Days to Decision 48 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary

Device Classification

Product Code GMQ — Antigens, Nontreponemal, All
Device Class Class II — Special Controls
CFR Regulation 21 CFR 866.3820

Similar Devices — GMQ Antigens, Nontreponemal, All

All 31
Gold Standard Diagnostics (GSD) AIX1000 Rapid Plasma Reagin (RPR) Automated Test System
K250249 · Gold Standard Diagnostics, LLC · Oct 2025
ASI Automated RPR (rapid plasma reagin) Test for Syphilis, for use on the ASI Evolution Automated Syphilis Analyzer
K201438 · Arlington Scientific, Inc. (Asi) · Oct 2020
ASI Automated ASI RPR Test for Syphilis on the ASI Evolution
K182391 · Arlington Scientific, Inc. (Asi) · Nov 2018
ASI Evolution
K173376 · Arlington Scientific, Inc. (Asi) · Jun 2018
Gold Standard Diagnostics AIX1000 Rapid Plasma Reagin (RPR) Automated Test System
K150358 · Gold Standard Diagnostics · Nov 2015
THE DAYA SYPHILIS TEST/THE TRUST ANTIGEN TEST
K000687 · Beacon Biologicals, Inc. · Jun 2000