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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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glass vials MEDI-PLAST INTL., INC. k811269 06/16/1981
glide device HOME SKINOVATIONS LTD. k131870 08/14/2013
gould-statham sp1405 pressure monitor GOULD, INC. k780798 06/13/1978
graftys hbs GRAFTYS k082498 02/25/2009
guide wire for edi catheter, 8fr,125cm,5 each,guide wire for edi catheter, 8fr,125cm,5 each,guide wire for edi catheter, MAQUET CRITICAL CARE AB k101199 08/27/2010
guiding catheter Texas Medical Technologies, Inc. k153703 05/12/2016
gyrus ent somnoplasty generator GYRUS ENT L.L.C. k020067 04/04/2002
hbs headless bone screw SCHOENING & ASSOC., INC. k030302 08/08/2003
hcg-check DIAGNOSTIC TECHNOLOGY, INC. k831466 06/22/1983
headlights w/ filter-optico cables PILLING CO. k761142 01/05/1977

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