Qtest(R) Strep

FDA 510(k) K935667 · Becton Dickinson Advanced Diagnostics

Substantially Equivalent

510(k) numberK935667

Submission

Device name
Qtest(R) Strep
Applicant
Becton Dickinson Advanced Diagnostics
Sparks, MD, US
Received
November 26, 1993
Decision date
April 21, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

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

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K212623Healgen Strep A Rapid Test Strip (Throat Swab)GTY · Traditional Healgen Scientific,, LLC03/16/2022SE
K171976Sofia Strep A+ FIA, Sofia 2 AnalyzerGTY · Dual Track Quidel Corporation12/21/2017SE
K141775Sofia (R) Strep A+ FiaGTY · Dual Track Quidel Corporation12/16/2014SE
K133343Wondfo Rapid Strep a TestGTY · Traditional Guangzhou Wondfo Biotech Co., Ltd.01/31/2014SE
K123793Sofia Strep a FiaGTY · Traditional Quidel Corporation06/17/2013SE
K122718BD Veritor(Tm) System for Rapid Detection of Group a StrepGTY · Traditional Becton, Dickinson and Company02/06/2013SE
K091489Clearview Advanced Strep a , Model 737-430GTY · Traditional Binax, Inc.09/04/2009SE
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More from Princeton BioMeditech Corp.

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K931294Iq Tuptake AssayKHQ · Traditional 07/22/1993SE
K931295Iq TT4 AssayCDX · Traditional 07/20/1993SE
K926356Precise(Tm) Hcg(Urine/Serum) and Prcise(Tm) PregJHI · Traditional 03/18/1993SE
K925132Becton Dickinson Thyroid Stimulating Hormone SysteJLW · Traditional 12/28/1992SE
K923673Precise Strep aGTZ · Traditional 09/28/1992SE
K923060Iq Immunochemistry Sistem; Iq TSH AssayJJE · Traditional 09/15/1992SE
K914958Riatrac PlusJJY · Traditional 03/18/1992SE
K915197Precise TM HCGJHI · Traditional 12/17/1991SE
K915200Precise TM HCG for Use in the Physicians Office laJHI · Traditional 12/16/1991SE

Questions and answers

When was Qtest(R) Strep cleared by the FDA?

Qtest(R) Strep (K935667) received a 510(k) decision of Substantially Equivalent on April 21, 1994, 146 days after the submission was received.

What is the product code of K935667?

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