FDA 510(k) Applications Submitted by SANDRA GRUNWALD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K131932 | 06/27/2013 | APNEALINK PRO | RESMED GERMANY INC. |
| K103167 | 10/27/2010 | STELLAR 150 | RESMED GERMANY INC. |
| K143272 | 11/14/2014 | ApneaLink Air | RESMED GERMANY INC. |
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