Medical Device Manufacturer · US , Washington, Dc , DC

Endocross, Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2008

Recent clearances: ENABLER-P CATHETER SYSTEM, MODEL 3000, ENABLER-P CATHETER, 1000 PART NUMBER:1160, ENABLER-P SUPPORT CATHETER

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Endocross, Ltd. Cardiovascular ✕

3 devices

1-3 of 3

Cleared Dec 30, 2009

ENABLER-P CATHETER SYSTEM, MODEL 3000

Cardiovascular · 162d

Cleared May 22, 2009

ENABLER-P CATHETER, 1000 PART NUMBER:1160

Cardiovascular · 150d

Cleared Nov 20, 2008

ENABLER-P SUPPORT CATHETER

Cardiovascular · 98d