510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K895095Substantially Equivalent

Aks II

Amoco Technology Co., Naperville IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K895095 is the FDA 510(k) clearance record for AKS II, a class II device, cleared for Amoco Technology Co. on under FDA product code LNJ (Analyzer, Chromosome, Automated). FDA records list one 510(k) clearance for Amoco Technology Co. As of , FDA records show no recalls naming K895095.

Clearance record

Decision date
Received
(179 days to decision)
Product code
LNJ Analyzer, Chromosome, Automated
Regulation
21 CFR 864.5260
Device class
Class II
Review panel
Hematology
Applicant
Amoco Technology Co. Amoco Research Center, Naperville IL
Third party review
No

Clearances, product code LNJ

Trailing 12 months

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

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