Medical Device Manufacturer · US , Houston , TX

Endothelix, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2007

Recent clearances: VENDYS, MODEL 6000 B B/C, VENDYS MODEL 5000 B/BC

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Endothelix, Inc. Cardiovascular ✕

2 devices

1-2 of 2

Cleared Nov 02, 2007

VENDYS, MODEL 6000 B B/C

Cardiovascular · 18d

Cleared Aug 16, 2007

VENDYS MODEL 5000 B/BC

Cardiovascular · 493d