510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K060761Substantially Equivalent

Breathscan, Breath and Breath Check Alcohol Detectors

Akers Biosciences, Inc., Thorofare NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K060761 is the FDA 510(k) clearance record for BREATHSCAN, BREATH AND BREATH CHECK ALCOHOL DETECTORS, a class I device, cleared for Akers Biosciences, Inc. on under FDA product code DJZ (Devices, Breath Trapping, Alcohol). FDA records list 5 510(k) clearances for Akers Biosciences, Inc., from to . As of , FDA records show no recalls naming K060761.

Clearance record

Decision date
Received
(38 days to decision)
Product code
DJZ Devices, Breath Trapping, Alcohol
Regulation
21 CFR 862.3050
Device class
Class I
Review panel
Clinical Toxicology
Applicant
Akers Biosciences, Inc. 201 Grove Rd., Thorofare NJ
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