FDA 510(k) Applications Submitted by Pearl, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K243893 | 12/18/2024 | Second Opinion« Pediatric | Pearl, Inc. |
| K243989 | 12/26/2024 | Second Opinion« 3D | Pearl, Inc. |
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