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FDA 510(k) Application Details - K053061
Device Classification Name
Cyclosporine
More FDA Info for this Device
510(K) Number
K053061
Device Name
Cyclosporine
Applicant
DADE BEHRING, INC.
P.O. BOX 6101
M/S 514
NEWARK, DE 19714-6101 US
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Contact
YUK-TING LEWIS
Other 510(k) Applications for this Contact
Regulation Number
862.1235
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Classification Product Code
MKW
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More FDA Info for this Product Code
Date Received
10/31/2005
Decision Date
02/06/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
TX - Clinical Toxicology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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