ImmunoCard STAT! HpSA

FDA 510(k) K153661 · Meridian Bioscience, Inc.

Substantially Equivalent

510(k) numberK153661

Submission

Device name
ImmunoCard STAT! HpSA
Applicant
Meridian Bioscience, Inc.
Cincinnati, OH, US
Received
December 21, 2015
Decision date
March 14, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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
K183573Vstrip H. pylori Antigen Rapid TestLYR · Traditional Panion & BF Biotech, Inc.03/14/2019SE
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
K151935Alere Signify H. pylori Whole Blood, Serum, Plasma; Alere Signify H. pylori Whole Blood…LYR · Special Alere San Diego, Incorporated08/12/2015SE

More from Alere San Diego, Incorporated

510(k)DeviceDecision
K243922RevogeneOOI · Traditional 03/20/2025SE
K230901Premier HpSA Flex (619096)LYR · Traditional 07/03/2023SE
K222829Curian® Shiga ToxinGMZ · Traditional 04/17/2023SE
K222779RevogeneOOI · Special 01/26/2023SE
K220480RevogeneOOI · Traditional 07/11/2022SE
K210976Curian CampyLQP · Traditional 12/23/2021SE
K192817Curian HpSA, Curian AnalyzerLYR · Traditional 03/13/2020SE
K182559PREMIER Platinum HpSA PLUSLYR · Traditional 11/05/2018SE
K163273TRU LegionellaMJH · Special 02/21/2017SE
K160829illumigene Mycoplasma Direct DNA Amplification Assay, illumigene Mycoplasma Direct…OZX · Traditional 06/13/2016SE

Questions and answers

When was ImmunoCard STAT! HpSA cleared by the FDA?

ImmunoCard STAT! HpSA (K153661) received a 510(k) decision of Substantially Equivalent on March 14, 2016, 84 days after the submission was received.

What is the product code of K153661?

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