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. |
|
Device | HERCEPTEST |
Generic Name | SYSTEM, TEST, HER-2/NEU, IHC |
Applicant | Agilent Technologies Singapore (International) Pte Ltd. No. 1 Yishun Avenue 7 Singapore 76892 |
PMA Number | P980018 |
Supplement Number | S007 |
Date Received | 12/31/2009 |
Decision Date | 01/21/2010 |
Product Code |
MVC |
Advisory Committee |
Pathology |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | Yes |
Approval Order Statement CHANGES IN THE CONTROL SLIDES FOR THE HERCEPTEST¿ KIT. |
|
|