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C-KIT PHARMDX

FDA premarket approval P040011 · decided 2005-06-27

Approval details

PMA number
P040011
Trade name
C-KIT PHARMDX
Generic name
Immunohistochemistry antibody assay, c-kit
Applicant
Dako North America, Inc.
Date received
2004-03-12
Decision date
2005-06-27
Days to decision
472 days
Decision code
APWD
Product code
NKF
Advisory committee
Pathology
Expedited review
No
Location
Carpinteria, CA
Statement
APPROVAL FOR THE DAKOCYTOMATION C-KIT PHARMDX. DAKOCYTOMATION C-KIT PHARMDX ON THE DAKO AUTOSTAINER: THE C-KIT PHARMDX ASSAY IS A QUALITATIVE IMMUNOHISTOCHEMICAL (IHC) KIT SYSTEM USED ON THE DAKO AUTOSTAINER, FOR THE IDENTIFICATION OF C-KIT PROTEIN/CD117 ANTIGEN (C-KIT PROTEIN) EXPRESSION IN NORMAL AND NEOPLASTIC FORMALIN-FIXED PARAFFIN-EMBEDDED TISSUES FOR HISTOLOGICAL EVALUATION. THE C-KIT PHARMDX RABBIT POLYCLONAL ANTIBODIES SPECIFICALLY DETECT THE C-KIT PROTEIN IN CD117 ANTIGEN-EXPRESSING CE

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MONOCLONAL MOUSE ANTI-HUMAN PROGESTERONE RECEPTOR, CLONE PGR 636, READY-TO-USE (LINK) (K130861)Dako North America, Inc.2013-12-09
MONOCLONAL RABBIT ANTI-HUMAN ESTROGEN RECEPTOR (ER) A, CLONE EPI (K120663)Dako North America, Inc.2013-02-12
MONOCLONAL RABBIT ANTI HUMAN ESTROGEN RECEPTOR ALPHA ANTIBODY CLONE SP1, MODEL M3634 (K081286)Dako North America, Inc.2009-05-08