FDA 510(k) Applications Submitted by MARY KAY JENSEN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120880 | 03/23/2012 | ORBIT | NATIONAL BIOMEDICAL LLC DBA QRS DIAGNOSTIC |
| K031964 | 06/25/2003 | BPCARD | QRS DIAGNOSTIC, LLC. |
| K083749 | 12/17/2008 | CARDIOVIEW32 REVIEW MODULE | QRS DIAGNOSTIC, LLC. |
| K073630 | 12/26/2007 | MODIFICATION TO: BPCARD, MODEL Z-7000-0700 | QRS DIAGNOSTIC, LLC. |
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