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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 491 Results
ProductCode: FOZ Decision Date To: 01/23/2022
 
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Device Name
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510(K)
Number
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introcan safety iv catheter B.Braun Medical Inc. K220626 05/14/2022
hydromid 4f single lumen midline catheter Access Vascular, Inc. K220772 12/07/2022
bd cathena safety iv catheter Becton Dickinson Infusion Therapy Systems Inc. K220584 03/31/2022
cook® spectrum® 2 mrc central venous catheter Cook Advanced Technologies K223648 02/03/2023
introcan safety 2 iv catheter B.Braun Medical Inc. K220756 06/23/2022
b. braun introcan safety 2 iv catheter B. Braun Medical Inc. K213664 02/11/2022
pluski safe 1 safety iv catheter Mediplus (India) Limited K210037 03/25/2022
introcan safety 3 closed iv catheter B.Braun Medical Inc. K213085 10/25/2021
magicath ii Woo Young Medical Co., Ltd. K210929 09/13/2022
leaderflex mini and leaderflex nano Vygon USA K212370 08/29/2022
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