Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameCURESIS PLASMA SEPARATOR
Classification Nameseparator, automated, blood cell and plasma, therapeutic
Generic Nameplasma separator
ApplicantORGANON TEKNIKA CORP.
PMA NumberP830010
Supplement NumberS001
Date Received11/19/1984
Decision Date02/12/1985
Product Code
LKN[ Registered Establishments with LKN ]
Advisory Committee Gastroenterology/Urology
Expedited Review Granted? No
Combination Product No
-
-