FDA 510(k) Applications Submitted by Philips Respironics
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K233555 | 11/06/2023 | AF531 Oro-Nasal EE Leak 1 Face Mask; AF531 Oro-Nasal EE Leak 2 Face Mask | Philips Respironics |
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