Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K023617Substantially Equivalent

Dri Methadone Metabolite Enzyme Immunoassay

Microgenics Corporation, Fremont Blvd. CA / Traditional, Substantially Equivalent

K023617 is the FDA 510(k) clearance record for DRI METHADONE METABOLITE ENZYME IMMUNOASSAY, a class II device, cleared for Microgenics Corp. on under FDA product code DJR (Enzyme Immunoassay, Methadone). FDA records list 128 510(k) clearances for Microgenics Corp., from to . As of , FDA records show no recalls naming K023617.

Clearance record

Decision date
Received
(302 days to decision)
Product code
DJR Enzyme Immunoassay, Methadone
Regulation
21 CFR 862.3620
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Microgenics Corp. 46360 Fremont Blvd., Fremont Blvd. CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DJR

Trailing 12 months

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

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