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. General Hospital ✕
16 devices
Cleared
Mar 22, 1995
MAHURKAR DUAL LUMEN CATHETER
General Hospital
253d
Cleared
Mar 12, 1990
Q-PORT SYSTEM KIT
General Hospital
231d
Cleared
Aug 25, 1989
MODIFIED MATERIAL USED IN INFUSION T
General Hospital
87d
Cleared
Jan 31, 1989
MODIFIED 7 INCH CONTINUOUS INFUSION SETS
General Hospital
144d
Cleared
Oct 04, 1988
NON-CORING NEEDLES
General Hospital
77d
Cleared
Dec 29, 1987
A SERIES OF 7 INCH CONTINUOUS INFUSION SETS
General Hospital
62d
Cleared
Feb 25, 1987
INSTRUCTION CHANGE FOR RIGHT ATRIAL/RAAF CATHETER
General Hospital
82d
Cleared
May 17, 1985
QUINTON INJECTION SEALING CAP
General Hospital
199d
Cleared
Feb 15, 1985
QUINTON WHITE SEALING CAP
General Hospital
15d
Cleared
Nov 08, 1984
LUER LOCKING ADAPTER(MATERIAL CHANGE)
General Hospital
255d
Cleared
Mar 19, 1984
PEDIATRIC RIGHT ATRIAL CATHETER 1/3MM
General Hospital
166d
Cleared
Feb 13, 1984
RAAF DUAL LUMEN CATH. REPAIR KIT 2.2
General Hospital
69d
Cleared
Jan 03, 1984
RAAF CATHETER REPAIR KIT
General Hospital
154d
Cleared
Jan 03, 1984
REPAIR KITS FOR RIGHT ATRIAL CATH
General Hospital
140d
Cleared
Aug 08, 1983
INJECTION SEALING CAP 13791
General Hospital
167d
Cleared
Oct 02, 1981
QI 1150-1T INFUSION T
General Hospital
10d