FDA 510(k) Applications Submitted by Bouse Angela
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K241451 | 05/22/2024 | Rusch Endotracheal Tubes (Reinforced); Rusch Endotracheal Tubes (Safety Clear); Rusch Endotracheal Tubes (Safety Clear Pediatric) | Teleflex Incorporated |
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