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U.S. Department of Health and Human Services

510(k) Premarket Notification
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31 to 40 of 489 Results
ProductCode: FOZ Decision Date To: 01/23/2022
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Export all 489 Records to ExcelExport to Excel | Download Files | More About 510(k)
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deltaven xiv max, deltaven xiv max ff Delta Med SpA K171530 12/21/2017
bd nexiva diffusics closed iv catheter systems Becton Dickinson Infusion Therapy Systems, Inc. K173354 12/15/2017
bd cathena safety iv catheter Becton, Dickinson and Company K172506 09/17/2017
bd intima ii plus closed iv catheter system Becton, Dickinson and Company K172204 08/17/2017
introcan safety 3 closed iv catheter B.BRAUN MELSUNGEN AG K163358 04/28/2017
bd nexiva closed iv catheter system (single port) with maxzero needleless connector Becton, Dickinson and Company K170336 03/10/2017
nipro safetouch iv catheter NIPRO MEDICAL CORPORATION K161681 03/08/2017
bd nexiva diffusics closed iv catheter system Becton, Dickinson and Company K170283 02/28/2017
arrow endurance extended dwell peripheral catheter system Arrow International, Inc. (subsidiary of Teleflex Inc.) K163513 02/24/2017
accucath intravascular catheter C.R.BARD, INC. K162894 11/15/2016
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