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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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510(K)
Number
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Decision
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hdm97 IBP INSTRUMENTS GMBH k020908 05/22/2002
hdm99 IBP INSTRUMENTS GMBH k020909 05/22/2002
eclipse, helios option VARIAN MEDICAL SYSTEMS, INC. k021268 05/22/2002
magnetom symphony quadrature tx/rx head coil USA INSTRUMENTS, INC. k021262 05/21/2002
serralester SERRAL, S.A. DE C.V. k020902 05/20/2002
vector f series high-speed dental handpieces VECTOR RESEARCH & DEVELOPMENT k020113 05/17/2002
z3 guide catheter MEDTRONIC VASCULAR k021256 05/17/2002
ebi ais spine system EBI, L.P. k020887 05/16/2002
surgassist flexshaft 2, model fs2 14 POWER MEDICAL INTERVENTIONS, INC. k021249 05/15/2002
modification to sparc sling system AMERICAN MEDICAL SYSTEMS, INC. k021263 05/15/2002

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