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
FDA 510(k) Regulatory Record - Quinton, Inc. Gastroenterology & Urology ✕
51 devices
Cleared
Sep 13, 1996
MAHURKAR 8 FR DUAL LEMEN CATHETER
Gastroenterology & Urology
317d
Cleared
May 09, 1990
MODIFIED PERM-CATH
Gastroenterology & Urology
76d
Cleared
Jan 29, 1990
MODIFIED QUINTON SINGLE LUMEN CATHETER
Gastroenterology & Urology
91d
Cleared
Jun 08, 1989
QUINTON SINGLE LUMEN CATHETER
Gastroenterology & Urology
34d
Cleared
Mar 27, 1989
PERITONEAL CATHETERS WITH AN ADDED FUNCTION
Gastroenterology & Urology
67d
Cleared
Feb 22, 1988
MODIFIED FORMED-EXTENSION MAHURKAR DUAL LUMEN CATH
Gastroenterology & Urology
13d
Cleared
Feb 17, 1988
PERMCATH INSERTION TRAY
Gastroenterology & Urology
100d
Cleared
Dec 29, 1987
BENT NECK CURLCATH PERITONEAL DIALYSIS KIT
Gastroenterology & Urology
50d
Cleared
Dec 09, 1987
PERITONEAL DIALYSIS KIT (ACUTE AND CHRONIC FORM)
Gastroenterology & Urology
26d
Cleared
Jun 17, 1987
ADULT PERM-CATH 40CM.
Gastroenterology & Urology
43d
Cleared
Jun 17, 1987
PERM-CATH CATHETER KIT
Gastroenterology & Urology
29d
Cleared
May 18, 1987
MODIFIED USE OF PULL-APART INTRODUCER SET
Gastroenterology & Urology
13d
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