Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K020694Substantially Equivalent

Qab2a Igm Elisa Kit

Cheshire Diagnostics, Ltd., Cheshire, GB / Traditional, Substantially Equivalent

K020694 is the FDA 510(k) clearance record for QAB2A IGM ELISA KIT, a class II device, cleared for Cheshire Diagnostics , Ltd. on under FDA product code MVS (Kit, Typing, Hla-Dqb). FDA records list 6 510(k) clearances for Cheshire Diagnostics , Ltd., from to . As of , FDA records show no recalls naming K020694.

Clearance record

Decision date
Received
(46 days to decision)
Product code
MVS Kit, Typing, Hla-Dqb
Regulation
21 CFR 866.5660
Device class
Class II
Review panel
Immunology
Applicant
Cheshire Diagnostics , Ltd. Management Centre, Inward Way, Cheshire, GB
510(k) summary
Statement
Third party review
No

Clearances, product code MVS

Trailing 12 months

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

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