FDA 510(k) Applications Submitted by QUINTON, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K001492 05/12/2000 QUINTON Q-STRESS, MODEL 000483 QUINTON, INC.
K003576 11/20/2000 Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503 QUINTON, INC.
K021906 06/10/2002 QUINTON Q-CATH, MODEL 000460 QUINTON, INC.
K032038 07/01/2003 PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601 QUINTON, INC.
K955002 11/01/1995 MAHURKAR 8 FR DUAL LEMEN CATHETER QUINTON, INC.
K961014 03/13/1996 QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH QUINTON, INC.
K964784 11/27/1996 SYNERGY CARDIOLOGY INFORMATION SYSTEM (00431) QUINTON, INC.
K964978 12/12/1996 VITAL STATISTICS SYSTEM (O-CATH ACCESSORY) QUINTON, INC.
K990866 03/16/1999 QUINTON MEDTRACK CR PLUS TREADMILL QUINTON, INC.
K992908 08/30/1999 Q-TEL TELEMETRY SYSTEM V. 6.0 (ST) QUINTON, INC.
K971397 04/15/1997 VIEWCATH 3-D CATHETER PULLBACK QUINTON, INC.


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