Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K872180Substantially Equivalent

Kinetic 610 Ethanol

American Monitor Corp., Indianapolis IN / Traditional, Substantially Equivalent

K872180 is the FDA 510(k) clearance record for KINETIC 610 ETHANOL, a class II device, cleared for American Monitor Corp. on under FDA product code DML (Nad-Nadh, Specific Reagent For Alcohol Enzyme Method). FDA records list 73 510(k) clearances for American Monitor Corp., from to . As of , FDA records show no recalls naming K872180.

Clearance record

Decision date
Received
(29 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
American Monitor Corp. P.O. Box 68505, Indianapolis IN
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