Data / Medical devices / United States / AlcoPro Inc
AlcoPro Inc: FDA-registered device maker in Knoxville, TN, United States, 1 510(k) clearance
AlcoPro Inc is registered with the FDA (registration 1054127) in Knoxville, TN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 6, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1054127
- FEI number
- 1000112835
- Address
- 1626 Downtown West Boulevard, Knoxville, TN, United States, 37919
- Owner or operator
- AlcoPro Inc (10033291)
- Roles
- Manufacturer
- First device listed
- June 21, 2011
- Registered through
- 2026
- Brand names listed
- Alco-Breath Tube, BreathIQ, CheckPoint
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Devices, Breath Trapping, Alcohol | DJZ | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 6, 2011 | K102225 | ALCO-BREATH TUBE, CHECKPOINT BREATH ALCOHOL TEST | DJZ | Substantially Equivalent | Alcopro, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 6, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.