FDA 510(k) Applications Submitted by ESWALLOW USA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K092202 | 07/22/2009 | ESWALLOW DYSPHAGIA THERAPY KIT, PMI DYSPHAGIA THERAPY KIT | ESWALLOW USA |
| K113375 | 11/16/2011 | ESWALLOW USA ELECTRODE,ESWALLOW USA LEADWIRE | ESWALLOW USA |
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