510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K843211Substantially Equivalent

Amikacin Analytical Test Pack Aca

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

K843211 is the FDA 510(k) clearance record for AMIKACIN ANALYTICAL TEST PACK ACA, a class II device, cleared for E.I. Dupont DE Nemours & Co., Inc. on under FDA product code KLQ (Radioimmunoassay, Amikacin). 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 K843211.

Clearance record

Decision date
Received
(28 days to decision)
Product code
KLQ Radioimmunoassay, Amikacin
Regulation
21 CFR 862.3035
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 KLQ

Trailing 12 months

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

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