510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K812054Substantially Equivalent

Endab Digoxin Kit

IMMUNOTECH s.r.o., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K812054 is the FDA 510(k) clearance record for ENDAB DIGOXIN KIT, a class II device, cleared for Immunotech Corp. on under FDA product code KXT (Enzyme Immunoassay, Digoxin). FDA records list 42 510(k) clearances for IMMUNOTECH s.r.o., from to . As of , FDA records show no recalls naming K812054.

Clearance record

Decision date
Received
(22 days to decision)
Product code
KXT Enzyme Immunoassay, Digoxin
Regulation
21 CFR 862.3320
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Immunotech Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KXT

Trailing 12 months

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

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