Medical Device
Manufacturing
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K032057Substantially Equivalent

Toxcup Drug Screen Cup Amp/coc/met/opi/pcp/thc

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

K032057 is the FDA 510(k) clearance record for TOXCUP DRUG SCREEN CUP AMP/COC/MET/OPI/PCP/THC, a class II device, cleared for Branan Medical Corp. on under FDA product code DIO (Enzyme Immunoassay, Cocaine And Cocaine Metabolites). FDA records list 24 510(k) clearances for Branan Medical Corp., from to . As of , FDA records show 2 recalls naming K032057.

Clearance record

Decision date
Received
(50 days to decision)
Product code
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
Regulation
21 CFR 862.3250
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Branan Medical Corp. 10015 Muirlands Rd., Suite E, Irvine CA
510(k) summary
Statement
Third party review
No

Clearances, product code DIO

Trailing 12 months

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

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