FDA 510(k) Applications Submitted by Todd Korogi
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K171101 | 04/13/2017 | Closed Male Luer | Yukon Medical |
| K172631 | 09/01/2017 | Arisure Dry Spike | Yukon Medical |
| K172884 | 09/21/2017 | Arisure Closed Vial Adapter | Yukon Medical |
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