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FDA 510(k) Application Details - K970126
Device Classification Name
Radioimmunoassay, Estradiol
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510(K) Number
K970126
Device Name
Radioimmunoassay, Estradiol
Applicant
BIO-RAD LABORATORIES, INC.
1000 LAKE HAZELTINE DR.
CHASKA, MN 55318-1084 US
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Contact
SANDRA F SCHWARTZ, PH.D.
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Regulation Number
862.1260
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Classification Product Code
CHP
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More FDA Info for this Product Code
Date Received
01/14/1997
Decision Date
02/25/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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