510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K841532Substantially Equivalent

Aca Tricyclic Antidepressants Screen Tes

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

K841532 is the FDA 510(k) clearance record for ACA TRICYCLIC ANTIDEPRESSANTS SCREEN TES, a class II device, cleared for E.I. Dupont DE Nemours & Co., Inc. on under FDA product code LFG (Radioimmunoassay, Tricyclic Antidepressant Drugs). FDA's definition for product code LFG reads: "Intended to measure any of the tricyclic antidepressant drugs in serum or urine". 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 K841532.

Clearance record

Decision date
Received
(16 days to decision)
Product code
LFG Radioimmunoassay, Tricyclic Antidepressant Drugs
Regulation
21 CFR 862.3910
Device class
Class II
Review panel
Clinical Toxicology
Applicant
E.I. Dupont DE Nemours & Co., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code LFG

Trailing 12 months

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

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