Medical Device Manufacturer · US , Mchenry , IL

Quinton, Inc. - FDA 510(k) Cleared Devices

164 submissions · 160 cleared · Since 1976

164

Total

160

Cleared

Denied

Quinton, Inc. has 160 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 160 cleared submissions from 1976 to 2003. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Quinton, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Quinton, Inc.

164 devices

1-12 of 164

1 2 3 4

Cleared Sep 05, 2003

PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601

K032038 · DQK

Cardiovascular · 66d

Cleared Sep 04, 2002

QUINTON Q-CATH, MODEL 000460

K021906 · DQK

Cardiovascular · 86d

Cleared Jan 25, 2001

Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503

K003576 · DSI

Cardiovascular · 66d

Cleared Aug 09, 2000

QUINTON Q-STRESS, MODEL 000483

K001492 · DPS

Cardiovascular · 89d

Cleared Mar 06, 2000

Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)

K992908 · DSI

Cardiovascular · 189d

Cleared Apr 29, 1999

QUINTON MEDTRACK CR PLUS TREADMILL

K990866 · ISD

Physical Medicine · 44d

Cleared Aug 25, 1997

VIEWCATH 3-D CATHETER PULLBACK

K971397 · ITX

Radiology · 132d

Cleared Aug 13, 1997

SYNERGY CARDIOLOGY INFORMATION SYSTEM (00431)

K964784 · DPS

Cardiovascular · 259d

Cleared May 21, 1997

VITAL STATISTICS SYSTEM (O-CATH ACCESSORY)

K964978 · DQA

Anesthesiology · 160d

Cleared Sep 13, 1996

MAHURKAR 8 FR DUAL LEMEN CATHETER

K955002 · MPB

Gastroenterology & Urology · 317d

Cleared Jul 31, 1996

QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH

K961014 · LOS

Cardiovascular · 140d

Cleared Jun 28, 1995

QUINTON MODEL 710 STRESS ELECTROCARDIOGRAPH

K945626 · DPS

Cardiovascular · 224d

1 2 3 4

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Quinton, Inc. - FDA 510(k) Cleared Devices

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