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FDA 510(k) Application Details - K960066
Device Classification Name
Radioimmunoassay, Acth
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510(K) Number
K960066
Device Name
Radioimmunoassay, Acth
Applicant
DIAGNOSTIC PRODUCTS CORP.
5700 WEST 96TH ST.
LOS ANGELES, CA 90045-5597 US
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Contact
EDWARD M LEVINE, PHD.
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Regulation Number
862.1025
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Classification Product Code
CKG
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More FDA Info for this Product Code
Date Received
01/05/1996
Decision Date
02/16/1996
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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