FDA 510(k) Applications Submitted by Julie Broderick
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K162332 | 08/19/2016 | Nexcore GI Insufflator | NEXCORE TECHNOLOGY, LLC |
| K011943 | 06/21/2001 | IMPRO VISE ABSORBABLE CEMENT FLOW RESTRICTOR | KENSEY NASH CORP. |
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