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U.S. Department of Health and Human Services

510(k) Premarket Notification
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51 to 60 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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supercath5 TOGO MEDIKIT CO., LTD. K140419 05/12/2014
braided high pressure catheter connector THE R GROUP K905415 08/12/1991
marhukar triple lumen catheter, model 12 fr THE KENDAL CO. K000087 03/17/2000
tfx medical safety needle with introducer TFX MEDICAL, INC. K000665 05/02/2000
surshield safety i.v. catheter TERUMO MEDICAL CORP. K082362 09/17/2008
terumo hybria closed system safety i.v. catheter TERUMO MEDICAL CORP. K082997 04/15/2009
terumo surflo etfe i.v. catheter TERUMO MEDICAL CORP. K854566 01/23/1986
terumo surflo flex i.v. catheter and terumo surflash i.v. catheter TERUMO MEDICAL CORP. K991406 06/16/1999
terumo surflo(r) i.v. catheter TERUMO MEDICAL CORP. K891087 06/23/1989
terumo surflash safety i.v. catheter TERUMO Corporation K122544 09/05/2012
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