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Quinton, Inc.

FDA 510(k) & PMA Approved Devices — 164 products

Total Devices164
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K032038 PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601DQK2003-09-05 View
510(k) K021906 QUINTON Q-CATH, MODEL 000460DQK2002-09-04 View
510(k) K003576 Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503DSI2001-01-25 View
510(k) K001492 QUINTON Q-STRESS, MODEL 000483DPS2000-08-09 View
510(k) K992908 Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)DSI2000-03-06 View
510(k) K990866 QUINTON MEDTRACK CR PLUS TREADMILLISD1999-04-29 View
510(k) K971397 VIEWCATH 3-D CATHETER PULLBACKITX1997-08-25 View
510(k) K964784 SYNERGY CARDIOLOGY INFORMATION SYSTEM (00431)DPS1997-08-13 View
510(k) K964978 VITAL STATISTICS SYSTEM (O-CATH ACCESSORY)DQA1997-05-21 View
510(k) K955002 MAHURKAR 8 FR DUAL LEMEN CATHETERMPB1996-09-13 View
510(k) K961014 QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPHLOS1996-07-31 View
510(k) K945626 QUINTON MODEL 710 STRESS ELECTROCARDIOGRAPHDPS1995-06-28 View
510(k) K943349 MAHURKAR DUAL LUMEN CATHETERFOZ1995-03-22 View
510(k) K922254 LUKENS 2-0 BRAIDED SILK SUTURESDQO1992-09-01 View
510(k) K910017 Q4500 STREE TEST MONITORDPS1991-11-05 View
510(k) K912227 MONARK ERGOMETERSISD1991-08-07 View
510(k) K910808 Q-SMART HOLTER SYSTEMSDSI1991-07-17 View
510(k) K911751 MEDTRACK TREADMILLIOL1991-05-29 View
510(k) K900835 MODIFIED PERM-CATHLFJ1990-05-09 View
510(k) K894650 Q-PORT SYSTEM KITLJT1990-03-12 View
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