510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K002418Substantially Equivalent

Branan Medical Corporation Monitect Morphine 300 Drug Screen Test, Model 133C and 133D

Branan Medical Corp., Irvine CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002418 is the FDA 510(k) clearance record for BRANAN MEDICAL CORPORATION MONITECT MORPHINE 300 DRUG SCREEN TEST, MODEL 133C AND 133D, a class II device, cleared for Branan Medical Corporation on under FDA product code DOE (Radioimmunoassay, Morphine (125-I), Goat Antibody Ammonium Sulfate Sep.). FDA records list 24 510(k) clearances for Branan Medical Corporation, from to . As of , FDA records show no recalls naming K002418.

Clearance record

Decision date
Received
(106 days to decision)
Product code
DOE Radioimmunoassay, Morphine (125-I), Goat Antibody Ammonium Sulfate Sep.
Regulation
21 CFR 862.3640
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Branan Medical Corporation 10015 Muirlands Rd., Suite E, Irvine CA
510(k) summary
Statement
Third party review
No

Clearances, product code DOE

Trailing 12 months

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

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