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 NameVITROS IMMUNODIAGNOSTIC PRODUCT HBSAG REAGENT PACK & CALIBRATOR & VITROS IMMUNODIAGNOSTIC PRODUCTS HBSAG CONFIRMATORY KI
Classification Nametest, hepatitis b (b core, be antigen, be antibody, b core igm)
Generic Namehepatitis b surface antigen assay/confirmatory kit
ApplicantORTHO-CLINICAL DIAGNOSTICS, INC.
PMA NumberP000044
Supplement NumberS020
Date Received02/02/2009
Decision Date10/23/2009
Product Code
LOM[ Registered Establishments with LOM ]
Advisory Committee Microbiology
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - component
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for revision of the intended use to include use of the vitros 5600 integrated system and vitros 3600 immunodiagnostic system with the vitros hbsag assay and the vitros hbsag confirmatory kit. These devices, as modified, will be marketed under the trade name vitros immunodiagnostic products hbsag reagent pack, vitros immunodiagnostic products hbsag calibrator and vitros immunodiagnostic products hbsag confirmatory kit and is indicated for: vitros immunodiagnostic products hbsag reagent pack: for the in vitro qualitative detection of hepatitis b surface antigen (hbsag) in human serum and plasma (heparin, edta, and sodium citrate) using the vitros eci/eciq immunodiagnostic systems, the vitros 3600 immunodiagnostic system and the vitros 5600 integrated system. Assay results, in conjunction with other serological and clinical information, may be used for the laboratory diagnosis of individuals with acute and chronic hepatitis b. In addition, this assay may be used to screen for hepatitis b infection in pregnant women to identify neonates who are at high risk of acquiring iibv during the perinatal period. Vitros immunodiagnostic products hbsag calibralor: for use in the calibration of the vitros eci/eciq immunodiagnostic systems, the vitros 3600 immunodiagnostic system and the vitros 5600 integrated system for the in vitro qualitative detection of hepatitis b surface antigen (hbsag) in human serum and plasma using vitros hbsag reagent packs. The vitros hbsag calibrator has been validated for use only on the vitros eci/eciq immunodiagnostic systems, the vitros 3600 immunodiagnostic system and the vitros 5600 integrated system with the vitros immunodiagnostic products anti-hbc reagent packs. (see approval order for additional approval information).
-
-