Alere Signify H. pylori Whole Blood, Serum, Plasma; Alere Signify H. pylori Whole Blood Only;Alere Clearview H. pylori Whole Blood, Serum, Plasma; Alere Clearview H. pylori Whole Blood Only

FDA 510(k) K151935 · Alere San Diego, Incorporated

Substantially Equivalent

510(k) numberK151935

Submission

Device name
Alere Signify H. pylori Whole Blood, Serum, Plasma; Alere Signify H. pylori Whole Blood Only;Alere Clearview H. pylori Whole Blood, Serum, Plasma; Alere Clearview H. pylori Whole Blood Only
Applicant
Alere San Diego, Incorporated
San Diego, CA, US
Received
July 14, 2015
Decision date
August 12, 2015
Decision
Substantially Equivalent (SESE)
Type
Special 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

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K183573Vstrip H. pylori Antigen Rapid TestLYR · Traditional Panion & BF Biotech, Inc.03/14/2019SE
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K181400H. Pylori Chek™LYR · Traditional Techlab, Inc.08/21/2018SE
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K153661ImmunoCard STAT! HpSALYR · Traditional Meridian Bioscience, Inc.03/14/2016SE

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Questions and answers

When was Alere Signify H. pylori Whole Blood, Serum, Plasma; Alere Signify H. pylori Whole Blood Only;Alere Clearview H. pylori Whole Blood, Serum, Plasma; Alere Clearview H. pylori Whole Blood Only cleared by the FDA?

Alere Signify H. pylori Whole Blood, Serum, Plasma; Alere Signify H. pylori Whole Blood Only;Alere Clearview H. pylori Whole Blood, Serum, Plasma; Alere Clearview H. pylori Whole Blood Only (K151935) received a 510(k) decision of Substantially Equivalent on August 12, 2015, 29 days after the submission was received.

What is the product code of K151935?

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