510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K884375Substantially Equivalent

Translumbar Aortography Needle Catheter

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

K884375 is the FDA 510(k) clearance record for TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER, a class II device, cleared for Argon Medical Corp. on under FDA product code DQR (Cannula, Catheter). FDA records list 28 510(k) clearances for Argon Medical Corp., from to . As of , FDA records show no recalls naming K884375.

Clearance record

Decision date
Received
(85 days to decision)
Product code
DQR Cannula, Catheter
Regulation
21 CFR 870.1300
Device class
Class II
Review panel
Cardiovascular
Applicant
Argon Medical Corp. 1445 Flat Creek Rd., Athens TX
Third party review
No

Clearances, product code DQR

Trailing 12 months

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

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