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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