FDA 510(k) Applications Submitted by BIOVIEW LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K040591 | 03/08/2004 | DUET SYSTEM | BIOVIEW LTD. |
| K050840 | 04/01/2005 | MODIFICATION TO DUET SYSTEM | BIOVIEW LTD. |
| K061602 | 06/08/2006 | DUET SYSTEM | BIOVIEW LTD. |
| K030192 | 01/21/2003 | DUET SYSTEM | BIOVIEW LTD. |
| K130775 | 03/20/2013 | DUET SYSTEM | BIOVIEW LTD. |
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