Quinton, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
164
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K032038PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601September 5, 2003
K021906QUINTON Q-CATH, MODEL 000460September 4, 2002
K003576Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503January 25, 2001
K001492QUINTON Q-STRESS, MODEL 000483August 9, 2000
K992908Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)March 6, 2000
K990866QUINTON MEDTRACK CR PLUS TREADMILLApril 29, 1999
K971397VIEWCATH 3-D CATHETER PULLBACKAugust 25, 1997
K964784SYNERGY CARDIOLOGY INFORMATION SYSTEM (00431)August 13, 1997
K964978VITAL STATISTICS SYSTEM (O-CATH ACCESSORY)May 21, 1997
K955002MAHURKAR 8 FR DUAL LEMEN CATHETERSeptember 13, 1996
K961014QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPHJuly 31, 1996
K945626QUINTON MODEL 710 STRESS ELECTROCARDIOGRAPHJune 28, 1995
K943349MAHURKAR DUAL LUMEN CATHETERMarch 22, 1995
K922254LUKENS 2-0 BRAIDED SILK SUTURESSeptember 1, 1992
K910017Q4500 STREE TEST MONITORNovember 5, 1991
K912227MONARK ERGOMETERSAugust 7, 1991
K910808Q-SMART HOLTER SYSTEMSJuly 17, 1991
K911751MEDTRACK TREADMILLMay 29, 1991
K900835MODIFIED PERM-CATHMay 9, 1990
K894650Q-PORT SYSTEM KITMarch 12, 1990