FDA 510(k) Applications Submitted by APIERON, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K083617 | 12/08/2008 | APIERON INSIGHT ENO SYSTEM | APIERON, INC. |
| K073265 | 11/20/2007 | APIERON INSIGHT EXHALED NITRIC OXIDE (ENO) SYSTEM | APIERON, INC. |
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