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

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 jak2 gene mutation detection test
De Novo Number DEN160028
Device Name ipsogen JAK2 RGQ PCR Kit
Requester
qiagen inc
19300 germantown road
germantown,  MD  20874
Contact lindsey howard
Regulation Number866.6070
Classification Product Code
PSU  
Date Received07/01/2016
Decision Date 03/27/2017
Decision granted (DENG)
Classification Advisory Committee Molecular Genetics
Review Advisory Committee Pathology
Reclassification Order Reclassification Order
FDA Review Decision Summary
Type Direct
-
-