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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 487 Results
ProductCode: FOZ Decision Date To: 01/23/2022
 
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Export all 487 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
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510(K)
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introcan safety 2 iv catheter B.Braun Medical Inc. K220756 06/23/2022
introcan safety iv catheter B.Braun Medical Inc. K220626 05/14/2022
bd cathena safety iv catheter Becton Dickinson Infusion Therapy Systems Inc. K220584 03/31/2022
pluski safe 1 safety iv catheter Mediplus (India) Limited K210037 03/25/2022
b. braun introcan safety 2 iv catheter B. Braun Medical Inc. K213664 02/11/2022
introcan safety 3 closed iv catheter B.Braun Medical Inc. K213085 10/25/2021
disposable iv catheter Shinva Ande Healthcare Apparatus Co., Ltd. K202060 07/23/2021
bd intima ii closed iv catheter system, bd intima ii plus closed iv catheter system Becton, Dickinson and Company K200891 06/02/2021
hydromid Access Vascular Inc. K203069 02/08/2021
bd insyte autoguard shielded iv catheter, bd insyte autoguard bc shielded iv catheter, bd insyte autoguard bc pro shielded iv catheter Becton, Dickinson and Company K201075 12/18/2020
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