Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K151203Substantially Equivalent

Immunalysis Cannabinoids Urine Enzyme Immunoassay, Immunalysis cTHC Urine Calibrators, Immunalysis cTHC Urine Control Set

Immunalysis Corporation, Pomona CA / Traditional, Substantially Equivalent

K151203 is the FDA 510(k) clearance record for Immunalysis Cannabinoids Urine Enzyme Immunoassay, Immunalysis cTHC Urine Calibrators, Immunalysis cTHC Urine Control Set, a class II device, cleared for Immunalysis Corporation on under FDA product code LDJ (Enzyme Immunoassay, Cannabinoids). FDA records list 50 510(k) clearances for Immunalysis Corporation, from to . As of , FDA records show no recalls naming K151203.

Clearance record

Decision date
Received
(31 days to decision)
Product code
LDJ Enzyme Immunoassay, Cannabinoids
Regulation
21 CFR 862.3870
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Immunalysis Corporation 829 Towne Center Dr., Pomona CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LDJ

Trailing 12 months

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

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