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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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