FDA 510(k) Applications Submitted by Katie Dillon
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120543 | 02/23/2012 | TANDEMHEART FEMORAL ARTERIAL CANNULA SET | CARDIACASSIST INC. |
| K182276 | 08/22/2018 | MEDRAD MRXperion MR Injection System and MR Injection System Syringe Kit | Bayer Medical Care Inc. |
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