Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K973726Substantially Equivalent

Fingerprint Drug Screening Device

Applied Technology Ventures, LLC, Herndon VA / Traditional, Substantially Equivalent

K973726 is the FDA 510(k) clearance record for FINGERPRINT DRUG SCREENING DEVICE, a class II device, cleared for Applied Technology Ventures, LLC on under FDA product code DKZ (Enzyme Immunoassay, Amphetamine). FDA records list 2 510(k) clearances for Applied Technology Ventures, LLC, from to . As of , FDA records show no recalls naming K973726.

Clearance record

Decision date
Received
(37 days to decision)
Product code
DKZ Enzyme Immunoassay, Amphetamine
Regulation
21 CFR 862.3100
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Applied Technology Ventures, LLC 2190 Fox Mill Rd., Suite 200, Herndon VA
510(k) summary
Statement
Third party review
No

Clearances, product code DKZ

Trailing 12 months

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

FDA records show no clearances under product code DKZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DKZ, 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