Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K080848Substantially Equivalent

Alcohawk Model Pt500 Digital Alcohol Detector

Q3 Innovations, LLC, Deer Field IL / Traditional, Substantially Equivalent

K080848 is the FDA 510(k) clearance record for ALCOHAWK MODEL PT500 DIGITAL ALCOHOL DETECTOR, a class I device, cleared for Q3 Innovations, LLC on under FDA product code DJZ (Devices, Breath Trapping, Alcohol). FDA records list 2 510(k) clearances for Q3 Innovations, LLC, from to . As of , FDA records show no recalls naming K080848.

Clearance record

Decision date
Received
(121 days to decision)
Product code
DJZ Devices, Breath Trapping, Alcohol
Regulation
21 CFR 862.3050
Device class
Class I
Review panel
Clinical Toxicology
Applicant
Q3 Innovations, LLC P.O. Box 7007, Deer Field IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DJZ

Trailing 12 months

FDA records hold no clearances under product code DJZ in the trailing twelve months.

FDA records show no clearances under product code DJZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DJZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260