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) | 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 Biologics Premarket Approvals (PMAs) 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.
 
Device INTERCEPT(R) Blood Systerm for Platelets
Classification Nameilluminator system for blood products
Generic Namepreparation and storage of pathogen-reduced, blood components.
Applicant
Cerus Corporation
2550 stanwell drive
Concord , CA 94520 
PMA NumberBP140143
Supplement NumberS322
Date Received04/28/2017
Decision Date07/17/2018
Decision Approved
Product Code
PJF[ Registered Establishments with PJF ]
Advisory Committee Hematology
Supplement TypeNormal 180 Day Track
Expedited Review Granted? No
Third Party Review Elligble? No
Combination ProductNo
-
-