Medical Device Manufacturer · US , Mountain View , CA

Percutaneous Systems, Incorporated - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2005

Recent clearances: COAXIAL ACCORDION ERCP DEVICE, MODELS C0AC19001, COAC20005, COAC22003, EXPRESSWAY INTERMITTENT CATHETER, CYSTOGLIDE INTRODUCER SHEATH

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Percutaneous Systems, Incorporated Gastroenterology & Urology ✕

5 devices

1-5 of 5

Cleared Jul 22, 2009

COAXIAL ACCORDION ERCP DEVICE, MODELS C0AC19001, COAC20005, COAC22003

Gastroenterology & Urology · 147d

Cleared Mar 09, 2007

EXPRESSWAY INTERMITTENT CATHETER

Gastroenterology & Urology · 260d

Cleared Dec 12, 2006

CYSTOGLIDE INTRODUCER SHEATH

Gastroenterology & Urology · 476d

Cleared Sep 13, 2005

Gastroenterology & Urology · 46d

Cleared Feb 01, 2005

UPDATED SLIP UROLOGY INTRODUCER SHEATH

Gastroenterology & Urology · 137d