510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K830150Substantially Equivalent

Veinprep Vein Graft Prep. Kit A277723

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

K830150 is the FDA 510(k) clearance record for VEINPREP VEIN GRAFT PREP. KIT A277723, a class II device, cleared for Atrium Medical Corp. on under FDA product code DWD (Suction Control, Intracardiac, Cardiopulmonary Bypass). FDA records list 69 510(k) clearances for Atrium Medical Corp., from to . As of , FDA records show no recalls naming K830150.

Clearance record

Decision date
Received
(42 days to decision)
Product code
DWD Suction Control, Intracardiac, Cardiopulmonary Bypass
Regulation
21 CFR 870.4430
Device class
Class II
Review panel
Cardiovascular
Applicant
Atrium Medical Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DWD

Trailing 12 months

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

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