Vstrip H. pylori Antigen Rapid Test

FDA 510(k) K183573 · Panion & BF Biotech, Inc.

Substantially Equivalent

510(k) numberK183573

Submission

Device name
Vstrip H. pylori Antigen Rapid Test
Applicant
Panion & BF Biotech, Inc.
New Taipei City, TW
Received
December 21, 2018
Decision date
March 14, 2019
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LYR – Helicobacter Pylori
Device class
Class I (low risk)
Regulation
21 CFR 866.3110
Specialty
Microbiology

Other 510(k)s with product code LYR

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K232892Hp Detect™ Stool Antigen ELISALYR · Traditional Biomerica, Inc.12/15/2023SE
K230901Premier HpSA Flex (619096)LYR · Traditional Meridian Bioscience, Inc.07/03/2023SE
K192817Curian HpSA, Curian AnalyzerLYR · Traditional Meridian Bioscience, Inc.03/13/2020SE
K182559PREMIER Platinum HpSA PLUSLYR · Traditional Meridian Bioscience, Inc.11/05/2018SE
K181464LIAISON Helicobacter Antigen, LIAISON Helicobacter Antigen Control SetLYR · Traditional DiaSorin, Inc.08/31/2018SE
K181400H. Pylori Chek™LYR · Traditional Techlab, Inc.08/21/2018SE
K181379H. Pylori Quik ChekLYR · Traditional Techlab, Inc.08/21/2018SE
K161139LIAISON H. pylori IgG, LIAISON H. pylori IgG Control SetLYR · Traditional DiaSorin, Inc.07/22/2016SE
K153661ImmunoCard STAT! HpSALYR · Traditional Meridian Bioscience, Inc.03/14/2016SE
K151935Alere Signify H. pylori Whole Blood, Serum, Plasma; Alere Signify H. pylori Whole Blood…LYR · Special Alere San Diego, Incorporated08/12/2015SE

Questions and answers

When was Vstrip H. pylori Antigen Rapid Test cleared by the FDA?

Vstrip H. pylori Antigen Rapid Test (K183573) received a 510(k) decision of Substantially Equivalent on March 14, 2019, 83 days after the submission was received.

What is the product code of K183573?

The FDA product code is LYR – Helicobacter Pylori, a Class I (low risk) device regulated under 21 CFR 866.3110.