510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K812622Substantially Equivalent

Hemodialysis Venous & Arterial Set

Amisco Trading Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K812622 is the FDA 510(k) clearance record for HEMODIALYSIS VENOUS & ARTERIAL SET, a class II device, cleared for Amisco Trading Corp. on under FDA product code FKH (Solution-Test Standard-Conductivity, Dialysis). FDA records list 2 510(k) clearances for Amisco Trading Corp. As of , FDA records show no recalls naming K812622.

Clearance record

Decision date
Received
(9 days to decision)
Product code
FKH Solution-Test Standard-Conductivity, Dialysis
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Amisco Trading Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FKH

Trailing 12 months

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

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