510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K904115Substantially Equivalent

Hycor Accupinch Methamphetamine Test

Hycor Biomedical, Garden Grove CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K904115 is the FDA 510(k) clearance record for HYCOR ACCUPINCH METHAMPHETAMINE TEST, a class II device, cleared for Hycor Biomedical, Inc. on under FDA product code DKZ (Enzyme Immunoassay, Amphetamine). FDA records list 66 510(k) clearances for Hycor Biomedical, Inc., from to . As of , FDA records show no recalls naming K904115.

Clearance record

Decision date
Received
(83 days to decision)
Product code
DKZ Enzyme Immunoassay, Amphetamine
Regulation
21 CFR 862.3100
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Hycor Biomedical, Inc. 7272 Chapman Ave., Garden Grove CA
Third party review
No

Clearances, product code DKZ

Trailing 12 months

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

FDA records show no clearances under product code DKZ in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DKZ, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260