Percutaneous Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ACCORDION STONE MANAGEMENT DEVICE MODEL AC281205 AND AC3814510, COAXIAL ACCORDION STONE MANAGEMENT DEVICE, MODEL: COAC12005 - COA20015, CYSTOGLIDE DILATING INTRODUCER SHEATH
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Percutaneous Systems, Inc. Gastroenterology & Urology ✕
6 devices
Cleared
May 16, 2011
ACCORDION STONE MANAGEMENT DEVICE MODEL AC281205 AND AC3814510
Gastroenterology & Urology
228d
Cleared
Nov 13, 2008
COAXIAL ACCORDION STONE MANAGEMENT DEVICE, MODEL: COAC12005 - COA20015
Gastroenterology & Urology
50d
Cleared
Sep 22, 2005
CYSTOGLIDE DILATING INTRODUCER SHEATH
Gastroenterology & Urology
48d
Cleared
Nov 16, 2004
MICROVERTER URETERAL ACCESS SHEATH
Gastroenterology & Urology
29d
Cleared
May 20, 2004
SLIP UROLOGY CATHETER
Gastroenterology & Urology
83d
Cleared
May 20, 2004
SLIP UROLOGY INTRODUCER SHEATH
Gastroenterology & Urology
83d