FDA 510(k) Applications Submitted by Cadwell Industries, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K180269 01/31/2018 Cadwell Apollo System Cadwell Industries, Inc.
K181466 06/04/2018 Cadwell Zenith System Cadwell Industries, Inc.
K201819 07/01/2020 Cadwell Apollo System Cadwell Industries, Inc.
K162383 08/25/2016 Cadwell Sierra Summit, Cadwell Sierra Ascent CADWELL INDUSTRIES, INC.
K190760 03/25/2019 Cadwell Bolt Software Cadwell Industries, Inc.
K192624 09/23/2019 ApneaTrak Cadwell Industries, Inc.
K230415 02/16/2023 Cadwell Guardian Cadwell Industries, Inc.
K161027 04/12/2016 Cadwell AmpliScan Cadwell Industries, Inc.
K133355 10/31/2013 CADWELL FLEX EEG/PSG CADWELL INDUSTRIES, INC.
K162199 08/05/2016 Cascade IOMAX Intraoperative Monitor CADWELL INDUSTRIES, INC.


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