Healgen Strep A Rapid Test Strip (Throat Swab)

FDA 510(k) K212623 · Healgen Scientific,, LLC

Substantially Equivalent

510(k) numberK212623

Submission

Device name
Healgen Strep A Rapid Test Strip (Throat Swab)
Applicant
Healgen Scientific,, LLC
Bellaire, TX, US
Received
August 18, 2021
Decision date
March 16, 2022
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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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
K082661Biostrep a, Biosign Strep a, Statusfirst Strep aGTY · Special Princeton BioMeditech Corp.10/06/2008SE
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Questions and answers

When was Healgen Strep A Rapid Test Strip (Throat Swab) cleared by the FDA?

Healgen Strep A Rapid Test Strip (Throat Swab) (K212623) received a 510(k) decision of Substantially Equivalent on March 16, 2022, 210 days after the submission was received.

What is the product code of K212623?

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