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U.S. Department of Health and Human Services

510(K) Premarket Notification
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261 to 270 of 500 Results *
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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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neuro ii INNOVATIVE MAGNETIC RESONANCE IMAGING SYSTEMS INC. k002964 12/19/2000
friendly light er:yag pulsed laser INNOTECH USA, INC. k000023 11/06/2000
invigra male latex condom green colored and mint flavored INDUS MEDICARE LTD. k000038 03/21/2000
invigra male latex condom yellow colored and banana flavored INDUS MEDICARE LTD. k000039 03/21/2000
invigra male latex condom blue colored and vanilla flavored INDUS MEDICARE LTD. k000040 03/21/2000
crit-line monitor iii (clm iii) IN-LINE DIAGNOSTICS CORP. k001763 12/20/2000
impra carboflo vascular graft, impra carboflo vascular grafts for a-v access IMPRA, INC. k004011 03/27/2001
impra carboflo eptfe vascular grafts IMPRA, INC. k004012 05/14/2001
hedrocel revision cup, model 02-2yy-zzzz IMPLEX CORP. k001759 08/24/2000
implex continuum knee system-patellar components, model 04-xx-yyyyy IMPLEX CORP. k004013 01/25/2001

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