FDA 510(k) Applications Submitted by RESMED SAS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K113201 | 10/31/2011 | NARVAL CC | RESMED SAS |
| K143623 | 12/22/2014 | Narval Brux | RESMED SAS |
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