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FDA 510(k) Applications Submitted by QRS DIAGNOSTIC, LLC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030535
02/20/2003
EKGCARD SYSTEM
QRS DIAGNOSTIC, LLC.
K001278
04/21/2000
SENSAIRE DIAGNOSTIC SPIROMETER
QRS DIAGNOSTIC, LLC.
K001995
06/30/2000
SPIROXCARD DIAGNOSTIC SPIROMETER AND PULSE OXIMETER
QRS DIAGNOSTIC, LLC.
K973138
08/21/1997
SPIROCARD
QRS DIAGNOSTIC, LLC.
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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