Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K110830Substantially Equivalent

Elitech Clinical Systems Calcium Arsenazo; Elitech Clinical Systems Albumin; Elitech Clinical Systems Elical 2; Elitech

ELITechGroup Inc, Bothell WA / Traditional, Substantially Equivalent

K110830 is the FDA 510(k) clearance record for ELITECH CLINICAL SYSTEMS CALCIUM ARSENAZO; ELITECH CLINICAL SYSTEMS ALBUMIN; ELITECH CLINICAL SYSTEMS ELICAL 2; ELITECH, a class II device, cleared for Elitechgroup on under FDA product code CIX (Bromcresol Green Dye-Binding, Albumin). FDA records list 32 510(k) clearances for Elitechgroup, from to . As of , FDA records show one recall naming K110830.

Clearance record

Decision date
Received
(88 days to decision)
Product code
CIX Bromcresol Green Dye-Binding, Albumin
Regulation
21 CFR 862.1035
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Elitechgroup 21720 23rd Dr. SE Suite 150, Bothell WA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CIX

Trailing 12 months
1 clearance under product code CIX in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CIX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260