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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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dw 276 #3 IVOCLAR NORTH AMERICA, INC. k003635 12/22/2000
nucamma bi90 IS2 RESEARCH, INC. k003882 02/21/2001
suturegroove weight sizing set IOP, INC. k003646 02/22/2001
sperm wash medium, cat# 2003/2005 INVITROCARE, INC. k000989 06/08/2000
action af-1 wheelchair INVACARE CORP. k000174 02/18/2000
intuitive surgical da vinci endoscopic control system INTUITIVE SURGICAL, INC. k002489 03/02/2001
synergy vls cap nut models 2206, 6102 INTERPORE CROSS INTL. k000236 02/16/2000
hemochron kaolin-activated heparin and protamine dosing assays INTERNATIONAL TECHNIDYNE CORP. k010193 06/06/2001
biopatch antimicrobial dressing INTEGRA LIFESCIENCES CORP. k003229 10/26/2001
acl 9000 system INSTRUMENTATION LABORATORY CO. k000053 03/15/2000

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