Qrs Diagnostic, LLC is one of 20410 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Qrs Diagnostic, LLC - FDA 510(k) Cleared Devices
Recent clearances: CARDIOVIEW32 REVIEW MODULE, MODIFICATION TO: BPCARD, MODEL Z-7000-0700, BPCARD
7
Total
7
Cleared
0
Denied
Qrs Diagnostic, LLC has 7 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 7 cleared submissions from 1998 to 2009. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Qrs Diagnostic, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bsi Healthcare as regulatory consultant.
FDA 510(k) Regulatory Record - Qrs Diagnostic, LLC
7 devices
Cleared
Mar 10, 2009
CARDIOVIEW32 REVIEW MODULE
Cardiovascular
83d
Cleared
Jan 11, 2008
MODIFICATION TO: BPCARD, MODEL Z-7000-0700
Cardiovascular
16d
Cleared
Sep 05, 2003
BPCARD
Cardiovascular
72d
Cleared
Jun 11, 2003
EKGCARD SYSTEM
Cardiovascular
111d
Cleared
Nov 29, 2000
SENSAIRE DIAGNOSTIC SPIROMETER
Anesthesiology
222d
Cleared
Sep 08, 2000
SPIROXCARD DIAGNOSTIC SPIROMETER AND PULSE OXIMETER
Anesthesiology
70d
Cleared
Oct 28, 1998
SPIROCARD
Anesthesiology
433d