510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K842387Substantially Equivalent

Aca Benzodiazepines Screen Test Pk

E.I. Dupont de Nemours & Co., Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K842387 is the FDA 510(k) clearance record for ACA BENZODIAZEPINES SCREEN TEST PK, a class II device, cleared for E.I. Dupont DE Nemours & Co., Inc. on under FDA product code JXM (Enzyme Immunoassay, Benzodiazepine). FDA records list 253 510(k) clearances for E.I. Dupont DE Nemours & Co., Inc., from to . As of , FDA records show no recalls naming K842387.

Clearance record

Decision date
Received
(58 days to decision)
Product code
JXM Enzyme Immunoassay, Benzodiazepine
Regulation
21 CFR 862.3170
Device class
Class II
Review panel
Clinical Toxicology
Applicant
E.I. Dupont DE Nemours & Co., Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code JXM

Trailing 12 months

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

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