FDA 510(k) Applications Submitted by Covidien LLC( Formerly Beacon Endoscopic Corp.)
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150891 | 04/02/2015 | BNX Fine Needle Aspiration System and SharkCore LG Fine Needle Biopsy System | Covidien LLC( Formerly Beacon Endoscopic Corp.) |
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