Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K122633Substantially Equivalent

Toxcup Drug Screen Cup

Branan Medical Corp., Irvine CA / Traditional, Substantially Equivalent

K122633 is the FDA 510(k) clearance record for TOXCUP DRUG SCREEN CUP, a class II device, cleared for Branan Medical Corp. on under FDA product code LDJ (Enzyme Immunoassay, Cannabinoids). FDA records list 24 510(k) clearances for Branan Medical Corp., from to . As of , FDA records show 8 recalls naming K122633.

Clearance record

Decision date
Received
(162 days to decision)
Product code
LDJ Enzyme Immunoassay, Cannabinoids
Regulation
21 CFR 862.3870
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Branan Medical Corp. 140 Technology Dr. Suite 400, Irvine 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