• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Import Refusal Report

  • Print
  • Share
  • E-mail
-

Refusal Actions by FDA as Recorded in OASIS

for 74-Cardiovascular


Entry/doc/line/sfx Refusal Date Product
Code
Manufacturer
FEI
Manufacturer
Name
Manufacturer
Country/Area
112-7387005-9/1/1 14-Jul-2010 74DPS 3007305624 GUANGDONG BIOLIGHT MEDITECH CO., LTD China
 
112-7387005-9/1/2 14-Jul-2010 74DPS 3007305624 GUANGDONG BIOLIGHT MEDITECH CO., LTD China
 
112-7765054-9/1/1 21-Jul-2010 74DPS 3003675391 Cardionics Sa Belgium
 
112-9252986-7/1/1 22-Jul-2010 74DRO 3007852400 Sil Pro United States
 
004-5569797-9/1/1 08-Jul-2010 74DXF 1220452 Medtronic Vascular United States
 
112-7467346-0/1/1 09-Jul-2010 74DXK 3003675391 Cardionics Sa Belgium
 
406-0450278-7/1/1 01-Jul-2010 74DXN 3006704335 Panasonic Electric Works Wanbao China
 
112-7063075-3/1/1 08-Jul-2010 74DXN 3008321619 Nu Beca Maxcellent Taiwan
 
WCJ-0272728-4/1/1 14-Jul-2010 74DXQ 3003059812 Elitex Metal Group Mfg Corp. Taiwan
 
112-7632706-5/1/1 15-Jul-2010 74JOP 3003253206 Epoka Group Denmark
 
-
-