Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1054127

FEI Number

1000112835

Entity Name

AlcoPro Inc

City/State/Country

Knoxville, TN, US

Establishment Address

1626 Downtown West Boulevard, Knoxville, TN 37919, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

AlcoPro Inc (Owner Number: 10033291)

Owner / Operator Contact Address

2547 Sutherland Ave, Knoxville, TN 37919, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K102225

PMA Number

N/A

All Registered Proprietary Names

CheckPoint BreathIQ Alco-Breath Tube

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DJZ	Devices, Breath Trapping, Alcohol	Clinical Toxicology	Class 1	862.3050	2011-06-21

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AlcoPro Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1054127. Last updated year: 2026. Please use registration number 1054127 when referencing this establishment in official correspondence.