FDA 510(k) Applications Submitted by Patricia Dupe
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K141728 | 06/26/2014 | ACE CALIBRATOR | SENTINEL CH. SpA |
| K192118 | 08/06/2019 | CRP Vario | Sentinel CH, Spa |
| K193001 | 10/28/2019 | Albumin BCP | Sentinel CH. SpA |
| K173833 | 12/18/2017 | CRP Vario | SENTINEL CH. SpA |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact