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PyloPlus UBT System

FDA premarket approval P170022 · decided 2020-02-18

Approval details

PMA number
P170022
Trade name
PyloPlus UBT System
Generic name
Test, urea adult and pediatric (breath),
Applicant
Arj Medical, Inc.
Date received
2017-07-26
Decision date
2020-02-18
Days to decision
937 days
Decision code
APPR
Product code
OZA
Advisory committee
Microbiology
Expedited review
No
Location
Oldsmar, FL
Statement
Approval of the PyloPlus UBT.The PyloPlus UBT system is intended for use in the qualitative detection of urease associated with H. pylori in the human stomach and is indicated as an aid in the initial diagnosis of H. pylori infection in adults 18 years old and older. The PyloPlus UBT system consists of the PyloPlus UBT Kit and the PyloPlus UBT analyzer. The analyzer is an infrared Spectrometer used for the measurement of the ratio of 13CO2 to 12CO2 in breath samples. The PyloPlus UBT system is f

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510(k) clearances by this applicant

RecordFirmDate
URITEST 50 AND URITEST 500 URINE ANALYZER (K091472)Arj Medical, Inc.2010-04-27
URITEST 10 URINALYSIS REAGENT STRIPS (K052719)Arj Medical, Inc.2006-12-05
PYLO-PLUS (K052708)Arj Medical, Inc.2006-05-01