Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K013538Substantially Equivalent

Ethanol

Abbott Medical, Irving TX / Traditional, Substantially Equivalent

K013538 is the FDA 510(k) clearance record for ETHANOL, a class II device, cleared for Abbott Laboratories on under FDA product code DML (Nad-Nadh, Specific Reagent For Alcohol Enzyme Method). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show no recalls naming K013538.

Clearance record

Decision date
Received
(51 days to decision)
Product code
DML Nad-Nadh, Specific Reagent For Alcohol Enzyme Method
Regulation
21 CFR 862.3040
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Abbott Laboratories 1920 Hurd Dr., Ms 8-21, Irving TX
510(k) summary
Summary
Third party review
No

Clearances, product code DML

Trailing 12 months

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

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