Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information. |
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Device | ELECSYS ANTI-HBC |
Generic Name | Test, hepatitis b (b core, be antigen, be antibody, b core igm) |
Applicant | ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. INDIANAPOLIS, IN 46250 |
PMA Number | P100032 |
Supplement Number | S010 |
Date Received | 10/07/2015 |
Decision Date | 11/24/2015 |
Product Code |
LOM |
Advisory Committee |
Microbiology |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement A MODIFICATION TO AN IN-PROCESS TESTING PROCEDURE FOR THE SOLID PHASE COMPONENT USED IN THE ABOVE LISTED ELECSYS IMMUNOASSAYS. |
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