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
K842039Substantially Equivalent

Argon Dual Lumen Hemodialysis, Catheter

Argon Medical Corp., Athens TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K842039 is the FDA 510(k) clearance record for ARGON DUAL LUMEN HEMODIALYSIS, CATHETER, a class II device, cleared for Argon Medical Corp. on under FDA product code KNZ (Accessories, A-V Shunt). FDA records list 28 510(k) clearances for Argon Medical Corp., from to . As of , FDA records show no recalls naming K842039.

Clearance record

Decision date
Received
(253 days to decision)
Product code
KNZ Accessories, A-V Shunt
Regulation
21 CFR 876.5540
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Argon Medical Corp. P.O. Box 1970, Athens TX
Third party review
No

Clearances, product code KNZ

Trailing 12 months

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

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