Quinton, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Quinton, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601, QUINTON Q-CATH, MODEL 000460, Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503
164
Total
160
Cleared
0
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
Cleared
Sep 05, 2003
PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601
Cardiovascular
66d
Cleared
Sep 04, 2002
QUINTON Q-CATH, MODEL 000460
Cardiovascular
86d
Cleared
Jan 25, 2001
Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503
Cardiovascular
66d
Cleared
Aug 09, 2000
QUINTON Q-STRESS, MODEL 000483
Cardiovascular
89d
Cleared
Mar 06, 2000
Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)
Cardiovascular
189d
Cleared
Apr 29, 1999
QUINTON MEDTRACK CR PLUS TREADMILL
Physical Medicine
44d
Cleared
Aug 25, 1997
VIEWCATH 3-D CATHETER PULLBACK
Radiology
132d
Cleared
Aug 13, 1997
SYNERGY CARDIOLOGY INFORMATION SYSTEM (00431)
Cardiovascular
259d
Cleared
May 21, 1997
VITAL STATISTICS SYSTEM (O-CATH ACCESSORY)
Anesthesiology
160d
Cleared
Sep 13, 1996
MAHURKAR 8 FR DUAL LEMEN CATHETER
Gastroenterology & Urology
317d
Cleared
Jul 31, 1996
QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH
Cardiovascular
140d
Cleared
Jun 28, 1995
QUINTON MODEL 710 STRESS ELECTROCARDIOGRAPH
Cardiovascular
224d
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