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 | PATH VYSION HER-2 DNA PROBE KIT ASSAY |
Generic Name | SYSTEM, TEST, HER-2/NEU, NUCLEIC ACID OR SERUM |
Applicant | ABBOTT MOLECULAR, INC. 1300 EAST TOUHY AVENUE DES PLAINES, IL 60018 |
PMA Number | P980024 |
Supplement Number | S008 |
Date Received | 06/21/2012 |
Decision Date | 07/17/2012 |
Product Code |
MVD |
Advisory Committee |
Pathology |
Supplement Type | Special (Immediate Track) |
Supplement Reason | Labeling Change - Indications/instructions/shelf life/tradename |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement APPROVAL FOR CHANGES TO PATHVYSION LABELING IN ORDER TO PROVIDE CUSTOMERS WITH CONSISTENT, CURRENT, AND CLEAR INFORMATION. |
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