FDA 510(k) Applications Submitted by AprioMed AB
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150625 | 03/11/2015 | Morrison Steerable Needle | APRIOMED AB |
| K181756 | 07/02/2018 | Gangi-SoftGuard Coaxial Needle, Gangi-HydroGuard Coaxial Needle | AprioMed AB |
| K193268 | 11/26/2019 | APrioCore Plus | AprioMed AB |
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