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 | ABBOTT HBE (RDNA) EIA |
Generic Name | Test, hepatitis b (b core, be antigen, be antibody, b core igm) |
Applicant | Abbott Laboratories 100 ABBOTT PARK RD. DEPT: 09VA BLDG: AP6C-2 ABBOTT PARK, IL 60064-3500 |
PMA Number | P790025 |
Supplement Number | S008 |
Date Received | 12/18/2002 |
Decision Date | 01/17/2003 |
Withdrawal Date
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03/22/2007 |
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 CHANGES TO MANUFACTURING PROCESS, TEST METHOD ADDITIONS, AND SPECIFICATION CHANGES. |
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