FDA 510(k) Application Details - K844294

Device Classification Name Complement C1q, Antigen, Antiserum, Control

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510(K) Number K844294
Device Name Complement C1q, Antigen, Antiserum, Control
Applicant CORDIS CORP.
P.O. BOX 025700
MIAMI, FL US
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Contact SEYMOUR P HALBERT
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Regulation Number 866.5240

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Classification Product Code DAK
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Date Received 11/06/1984
Decision Date 02/04/1985
Decision SE - Substantially Equivalent
Classification Advisory Committee IM - Immunology
Review Advisory Committee IM - Immunology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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