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|Articles|December 1, 2008

Oncology

  • ONCOLOGY Vol 22 No 14
  • Volume 22
  • Issue 14

FDA Approves New Imaging System to Enhance Cervical Cancer Detection

BD Diagnostics recently announced that it received US Food and Drug Administration (FDA) Premarket Approval for the BD FocalPoint GS Imaging System.

BD Diagnostics recently announced that it received US Food and Drug Administration (FDA) Premarket Approval for the BD FocalPoint GS Imaging System. This innovative new system is designed to enhance cervical cancer screening for cytology laboratories using the BD SurePath Pap test slides to detect evidence of squamous carcinoma, adenocarcinoma and their usual precursor conditions.

Articles in this issue

over 17 years ago

The Absent-Minded Professor: An Unusual Complication of Melanoma

over 17 years ago

Inflammatory Breast Cancer: A Complex Disease

over 17 years ago

Defining the IBC Phenotype

over 17 years ago

Acupuncture

over 17 years ago

Two Orphan Drug Designations Granted for Reviroc in NHL

over 17 years ago

NDA Submitted for Trabectedin to Treat Relapsed Ovarian Cancer

over 17 years ago

FDA Considers Update for Tanning Bed Labels

over 17 years ago

Fostamatinib Is Well-Tolerated and Has Significant Clinical Activity in Diffuse Large B-Cell Lymphoma and Chronic Lymphocytic Leukemia

over 17 years ago

Dexamethasone in Induction Can Eliminate One-Third of All Relapses in Childhood Acute Lymphoblastic Leukemia

over 17 years ago

Novel Antifolate Pralatrexate Shows Promise in Patients With Relapsed or Refractory Peripheral T-Cell Lymphoma

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