Reditest Strep a Test Kit

FDA 510(k) K903194 · Boehringer Mannheim Corp.

Substantially Equivalent

510(k) numberK903194

Submission

Device name
Reditest Strep a Test Kit
Applicant
Boehringer Mannheim Corp.
Indianapolis, IN, US
Received
July 19, 1990
Decision date
August 22, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GTZ – Antisera, All Groups, Streptococcus Spp.
Device class
Class I (low risk)
Regulation
21 CFR 866.3740
Specialty
Microbiology

Other 510(k)s with product code GTZ

510(k)DeviceApplicantDecision
K012521Binax Now Streptococcus Pneumoniae TestGTZ · Traditional Binax, Inc.11/30/2001SE
K011709Uni-Gold Strep a Test KitGTZ · Traditional Trinity Biotech, Plc11/08/2001SE
K010523Modification to Binax Now Streptococcus Pneumoniae Urinary Antigen TestGTZ · Special Binax, Inc.03/15/2001SE
K991726Binax Nowr Streptococcus Pneumoniae Urinary Antigen Test (22 Test KIT),(12 Test Kit)…GTZ · Traditional Binax, Inc.08/27/1999SE
K971522Abbott Testpack Plus Strep a with on Board Controls (Obc) IIGTZ · Traditional Abbott Laboratories03/03/1998SE
K962060Strep a Oia MaxGTZ · Traditional Biostar, Inc.07/23/1997SE
K962296Streptolex-StatGTZ · Traditional Unipath , Ltd.12/16/1996SE
K961423Osom Strep a TestGTZ · Traditional Wyntek Diagnostics, Inc.10/11/1996SE
K962146Excel Onestep Group a Strep Antigen Module Test KitGTZ · Traditional Excel Scientific, Inc.10/07/1996SE
K955108Cards Q.S. Strep aGTZ · Traditional Quidel Corp.04/15/1996SE

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K984425Modification of Preciset Serum Proteins CalibratorJIX · Traditional 01/20/1999SE
K984372Elecsys Calcheck Troponin TJJY · Traditional 12/14/1998SE
K984105Elecsys Troponin T Stat TestMMI · Traditional 12/08/1998SE
K983503Roche Diagnostics, Boehringer Mannheim Corporation Inorganic Phosphorus Reagent Catalog…CEO · Traditional 12/01/1998SE
K983469Preciset Serum Proteins CalibratorJIX · Traditional 11/25/1998SE
K983185Boehringer Mannheim Tina-Quant Ige TestDGC · Traditional 11/12/1998SE
K983510Chemstrip 101 Urine AnalyzerKQO · Special 10/27/1998SE

Questions and answers

When was Reditest Strep a Test Kit cleared by the FDA?

Reditest Strep a Test Kit (K903194) received a 510(k) decision of Substantially Equivalent on August 22, 1990, 34 days after the submission was received.

What is the product code of K903194?

The FDA product code is GTZ – Antisera, All Groups, Streptococcus Spp., a Class I (low risk) device regulated under 21 CFR 866.3740.