Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K122066Substantially Equivalent

Human Beta-2 Microglobulin Urine Kit for Use on the Spaplus

The Binding Site Group Ltd., Birmingham, GB / Special, Substantially Equivalent

K122066 is the FDA 510(k) clearance record for HUMAN BETA-2 MICROGLOBULIN URINE KIT FOR USE ON THE SPAPLUS, a class II device, cleared for The Binding Site Group , Ltd. on under FDA product code JZG (System, Test, Beta-2-Microglobulin Immunological). FDA records list 44 510(k) clearances for The Binding Site Group , Ltd., from to . As of , FDA records show one recall naming K122066.

Clearance record

Decision date
Received
(45 days to decision)
Product code
JZG System, Test, Beta-2-Microglobulin Immunological
Regulation
21 CFR 866.5630
Device class
Class II
Review panel
Immunology
Applicant
The Binding Site Group , Ltd. 8 Calthorpe Rd., Birmingham, GB
510(k) summary
Statement
Third party review
No

Clearances, product code JZG

Trailing 12 months

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

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