• 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 VITROS Immunodiagnostic Products Anti-HIV 1+2 Calibrator; VITROS Immunodiagnostic Products Anti-HIV 1+2 Reagent Pack
Classification Nametest, hiv detection
Generic Namehiv detection test
Regulation Number866.3956
Applicant
Ortho-Clinical Diagnostics, Inc.
100 indigo creek drive
Rochester , NY 14626 -5101
PMA NumberBP050051
Supplement NumberS025
Date Received01/18/2011
Decision Date02/16/2011
Decision Approved
Product Code
MZF[ Registered Establishments with MZF ]
Advisory Committee Microbiology
Supplement Type30-Day Notice
Expedited Review Granted? No
Third Party Review Elligble? No
Combination ProductNo
-
-