Published in Blood Weekly, September 8th, 1997
The test received 510(k) clearance from the U.S. Food and Drug Administration (FDA) and is available in the U.S. to physicians to monitor their patients with metastatic breast cancer.
Chiron Diagnostics' ACS:180 BR is intended for use as an aid in the management of breast cancer patients with metastatic disease. The test allows clinicians to monitor the cancer's progression or regression in response to treatment. ACS:180 BR is an in vitro diagnostic test for the quantitative...
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Source: Blood Weekly (1997-09-08)
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