Shiley, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SHILEY PERFUSION TUBING SETS, SHILEY THERAPEUTIC AUTOTRANSFUSION SYSTEM, SHILEY PLEXUS(R) VENOUS RESERVOIR, PVR1200
174
Total
174
Cleared
0
Denied
FDA 510(k) Regulatory Record - Shiley, Inc. Gastroenterology & Urology ✕
8 devices
Cleared
Apr 27, 1988
MODIFIED SHILEY DUAL LUMEN SUBCLAVIAN CANNULA
Gastroenterology & Urology
30d
Cleared
Oct 02, 1986
MODIFIED SILICONE DUAL LUMEN SUBCLAVIAN CANNULA
Gastroenterology & Urology
10d
Cleared
Apr 23, 1986
SHILEY SILICONE DUAL LUMEN SUBCLAVIAN CANNULA
Gastroenterology & Urology
29d
Cleared
Jun 13, 1985
SHILEY SILICONE SUAL LUMEN SUBCLAVIAN CANNUAL
Gastroenterology & Urology
34d
Cleared
Apr 25, 1984
SINGLE LUMEN SUBCLAVIAN CANNULA
Gastroenterology & Urology
98d
Cleared
Dec 08, 1983
DUAL LUMEN SUBCLAVIAN CANNULA
Gastroenterology & Urology
34d
Cleared
Aug 03, 1982
SHIELY DUEL LUMEN SUBCLAVIAN CANNULA
Gastroenterology & Urology
14d
Cleared
Nov 19, 1976
PERFUSION TUBING SET
Gastroenterology & Urology
22d