FDA 510(k) Applications Submitted by Deb Fleetham
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K192238 | 08/19/2019 | AC3 Series Intra-Aortic Balloon Pump (IABP) | Arrow International, Teleflex |
| K142934 | 10/09/2014 | CrossCountry Transbronchial Access Tool straight, CrossCountry Transbronchial Access Tool curved | COVIDIEN |
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