510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K844586Substantially Equivalent

Il Genesis 21, Clinical Chemistry Analytical Sys

Instrumentation Laboratory Co., Lexington MA / Traditional, Substantially Equivalent

K844586 is the FDA 510(k) clearance record for IL GENESIS 21, CLINICAL CHEMISTRY ANALYTICAL SYS, a class I device, cleared for Instrumentation Laboratory CO on under FDA product code JJF (Analyzer, Chemistry, Micro, For Clinical Use). FDA records list 327 510(k) clearances for Instrumentation Laboratory CO, from to . As of , FDA records show no recalls naming K844586.

Clearance record

Decision date
Received
(18 days to decision)
Product code
JJF Analyzer, Chemistry, Micro, For Clinical Use
Regulation
21 CFR 862.2170
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Instrumentation Laboratory CO 113 Hartwell Ave., Lexington MA
Third party review
No

Clearances, product code JJF

Trailing 12 months

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

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