FDA 510(k) Applications Submitted by Philips India Limited
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K173187 | 10/02/2017 | MobileDiagnost M50 | Philips India Limited |
| K203623 | 12/11/2020 | StentBoost Mobile | Philips India Limited |
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