FDA 510(k) Applications Submitted by John Cadwell
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K161027 | 04/12/2016 | Cadwell AmpliScan | Cadwell Industries, Inc. |
| K133355 | 10/31/2013 | CADWELL FLEX EEG/PSG | CADWELL INDUSTRIES, INC. |
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