FDA 510(k) Applications Submitted by KELLEY BREHEIM
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120612 | 02/29/2012 | MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT | MEDTRONIC INC. |
| K212077 | 07/02/2021 | Teleflex Rusch SoftSimplastic Foley Catheters | Teleflex Medical, Inc. |
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