FDA 510(k) Applications Submitted by GENEXEL-SEIN, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K080853 | 03/26/2008 | DUO-CARE BLOOD GLUCOSE AND BLOOD PRESSURE MONITOR SYSTEM | GENEXEL-SEIN, INC. |
| K071523 | 06/04/2007 | FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR, MODELS BP1600, BP1650, BP1700 AND BP1750 | GENEXEL-SEIN, INC. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact