510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902475Substantially Equivalent

Cardio-Pak Angiography Custom Packs

Cardio-Pak, Billings MT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902475 is the FDA 510(k) clearance record for CARDIO-PAK ANGIOGRAPHY CUSTOM PACKS, a class II device, cleared for Cardio-Pak on under FDA product code DXT (Injector And Syringe, Angiographic). FDA records list one 510(k) clearance for Cardio-Pak. As of , FDA records show one recall naming K902475.

Clearance record

Decision date
Received
(182 days to decision)
Product code
DXT Injector And Syringe, Angiographic
Regulation
21 CFR 870.1650
Device class
Class II
Review panel
Cardiovascular
Applicant
Cardio-Pak 1602 4th Ave.North, Billings MT
Third party review
No

Clearances, product code DXT

Trailing 12 months
6 clearances under product code DXT in the twelve months to October 2026, May 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code DXT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20261
April 20261
May 20263
June 20260
July 20260
August 20260
September 20260
October 20260