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

Device Classification Under Section 513(f)(2)(De Novo)

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


New Search Back to Search Results
Device Classification Name anti-phospholipase a2 receptor
De Novo Number DEN140002
510(K) Number K132379
Device Name EUROIMMUN ANTI-PLA2R IFA
Requester
euroimmun us
1100 the american road
morris plains,  NJ  07950
Contact michael locke
Regulation Number866.5780
Classification Product Code
PGV  
Date Received03/28/2014
Decision Date 05/29/2014
Decision granted (DENG)
Classification Advisory Committee Microbiology
Review Advisory Committee Immunology
Classification Order Classification Order
FDA Review Decision Summary
Type Post-NSE
-
-