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U.S. Department of Health and Human Services

Import Refusal Report

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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
MH9-0024391-5/1/1 16-Jul-2003 74DPS 3003758059 Susuken Co Ltd Japan
 
F11-6216558-5/1/1 01-Jul-2003 74DQO 3002423263 Med-X International Inc United States
 
112-2365094-5/1/1 03-Jul-2003 74LIT 3003254770 Clearstream Technologies Ltd Ireland
 
004-9105688-3/1/1 25-Jul-2003 74MAL 2020394 Bard Peripheral Vascular Inc United States
 
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