Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K203833Substantially Equivalent

Tacrolimus Assay Kit

Shanghai Genext Medical Technology Co., Ltd., Shanghai, CN / Traditional, Substantially Equivalent

K203833 is the FDA 510(k) clearance record for Tacrolimus Assay Kit, a class II device, cleared for Shanghai Genext Medical Technology Co., Ltd. on under FDA product code MLM (Enzyme Immunoassay, Tracrolimus). FDA records list one 510(k) clearance for Shanghai Genext Medical Technology Co., Ltd. As of , FDA records show no recalls naming K203833.

Clearance record

Decision date
Received
(758 days to decision)
Product code
MLM Enzyme Immunoassay, Tracrolimus
Regulation
21 CFR 862.1678
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Shanghai Genext Medical Technology Co., Ltd. Rm1101, 11th Floor, Bldg. 2, Pujiang Hi-Tech Plz., #2388, Shanghai, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MLM

Trailing 12 months

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

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