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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