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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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pulpdent cavity preparation iii PULPDENT CORP. k994180 03/02/2000
pulpdent cavity preparation ii, pulpdent cavity preparation ii wuth fluoride PULPDENT CORP. k994181 02/29/2000
pulpdent cavity preparation 1, pulpdent cavity preparation 1 with fluoride PULPDENT CORP. k994182 02/23/2000
plr splined revision stem BIOMET, INC. k994184 02/15/2000
manual wheelchair MAJOR MOBILITY PRODUCTS, INC. k994185 01/13/2000
disetronic d-tron insulin infusion pump DISETRONIC MEDICAL SYSTEMS k994186 12/30/1999
synthes cervifix system SYNTHES (USA) k994187 12/21/1999
modification to agilent technologies anesthesia gas monitor, model m1026a #co5 AGILENT TECHNOLOGIES, GMBH k994188 05/19/2000
olympus creatine kinase reagent osr6179/6279 OLYMPUS DIAGNOSTICA GMBH k994189 01/20/2000
impregum garant l duosoft ESPE DENTAL AG k994190 01/27/2000

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