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U.S. Department of Health and Human Services

510(K) Premarket Notification
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Device Name
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Applicant
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510(K)
Number
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Decision
Date
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citrate buffer Bioscientific k811251 05/21/1981
circuflow 5200 sequential compression device Devon Medical, Inc. k101523 06/17/2010
ciba corning magic lite t3 immunoassay Ciba Corning Diagnostics Corp. k873945 11/23/1987
ceram-prime S & C Polymer GmbH k002502 11/08/2000
cavermap surgical aid Uromed Corp. k000507 04/21/2000
cardiac output measure system Cook, Inc. k831185 05/27/1983
capiox cr-cardiotomy reservoir Terumo Medical Corp. k821538 08/06/1982
cannulas Myocure, Inc. k880346 05/03/1988
candela vbeam pulse dye laser system Candela Corp. k033461 01/16/2004
calcium assay kit Diagnostic Chemicals, Ltd. (Usa) k842509 07/20/1984

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
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