FDA 510(k) Applications for Medical Device Product Code "HHI"
(System, Abortion, Vacuum)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K030935 | ACMI CORPORATION | BERKELEY V-10 VACUUM CURETTAGE SYSTEM | 06/23/2003 |
| K983181 | CYTOPREP INC. EST. | CYTOPREP | 11/16/1998 |
| K171440 | Gyrus ACMI | Berkeley VC-10 Vacuum Curettage System | 09/29/2017 |
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