FDA 510(k) Applications Submitted by KARMELSONIX
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090863 | 03/30/2009 | PERSONAL WHEEZOMETER | KARMELSONIX |
| K101022 | 04/13/2010 | PULMOTRACK 5050 WHOLTER, MODEL 5050 | KARMELSONIX |
| K102229 | 08/09/2010 | PULMOTRACK 2020 SYSTEM | KARMELSONIX |
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