Culturette Brand 10-MINUTE Group a Strep I.D.

FDA 510(k) K853073 · Marion Laboratories, Inc.

Substantially Equivalent

510(k) numberK853073

Submission

Device name
Culturette Brand 10-MINUTE Group a Strep I.D.
Applicant
Marion Laboratories, Inc.
Kansas City, MI, US
Received
July 23, 1985
Decision date
August 1, 1985
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

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K012521Binax Now Streptococcus Pneumoniae TestGTZ · Traditional Binax, Inc.11/30/2001SE
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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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K874554Enviclusive (TM)NAD · Traditional 03/11/1988SE
K874552Envisan PadKOZ · Traditional 01/22/1988SN
K874551Envinet(Tm)EFQ · Traditional 01/22/1988SN
K874553Envisan PasteKOZ · Traditional 12/18/1987SN
K870864Culturette Brand CDT Clostridium Difficile TestLLH · Traditional 04/14/1987SE
K863485Modification of Cdt(Tm) Clostridium TestLLH · Traditional 09/17/1986SE
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Questions and answers

When was Culturette Brand 10-MINUTE Group a Strep I.D. cleared by the FDA?

Culturette Brand 10-MINUTE Group a Strep I.D. (K853073) received a 510(k) decision of Substantially Equivalent on August 1, 1985, 9 days after the submission was received.

What is the product code of K853073?

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