510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K772369Substantially Equivalent

Needles Used in Angiographic Proced.

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

K772369 is the FDA 510(k) clearance record for NEEDLES USED IN ANGIOGRAPHIC PROCED., a class II device, cleared for Argon Medical Corp. on under FDA product code DRC (Trocar). FDA records list 28 510(k) clearances for Argon Medical Corp., from to . As of , FDA records show no recalls naming K772369.

Clearance record

Decision date
Received
(28 days to decision)
Product code
DRC Trocar
Regulation
21 CFR 870.1390
Device class
Class II
Review panel
Cardiovascular
Applicant
Argon Medical Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DRC

Trailing 12 months

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

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