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
K001520Substantially Equivalent

Alpha Omega Dual Cooler-Heater

Alpha Omega, Ltd., Austin TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K001520 is the FDA 510(k) clearance record for ALPHA OMEGA DUAL COOLER-HEATER, a class II device, cleared for Alpha Omega, Inc. on under FDA product code DWC (Controller, Temperature, Cardiopulmonary Bypass). FDA's definition for product code DWC reads: "If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at...". FDA records list 5 510(k) clearances for Alpha Omega, Inc., from to . As of , FDA records show no recalls naming K001520.

Clearance record

Decision date
Received
(190 days to decision)
Product code
DWC Controller, Temperature, Cardiopulmonary Bypass
Regulation
21 CFR 870.4250
Device class
Class II
Review panel
Cardiovascular
Applicant
Alpha Omega, Inc. 2525 Hartford Rd., Austin TX
510(k) summary
Summary
Third party review
No

Clearances, product code DWC

Trailing 12 months

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

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