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U.S. Department of Health and Human Services

510(k) Premarket Notification
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101 to 110 of 491 Results
ProductCode: FOZ Decision Date To: 01/23/2022
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510(K)
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snm firmgrip FLEXICATH LTD. K092629 09/25/2009
i.v. catheter, models: type i, type y, type straight WEIHAI JIERUI MEDICAL PRODUCTS CO., LTD. K083429 08/07/2009
bd l-cath single and dual lument catheters, midline catheter BECTON DICKINSON & CO. K091670 07/01/2009
terumo surshield safety i.v. catheter (18g x 51mm & 20g x 51mm sizes) TERUMO CORP. K090973 05/01/2009
terumo hybria closed system safety i.v. catheter TERUMO MEDICAL CORP. K082997 04/15/2009
supercath 5 TOGO MEDIKIT CO., LTD. K081953 03/12/2009
nova safe scalp vein blood collection set U.S. SAFETY SYRINGES CO., INC. K090502 03/10/2009
nuovoguard U.S. SAFETY SYRINGES CO., INC. K090122 02/05/2009
nuovocath U.S. SAFETY SYRINGES CO., INC. K083454 12/04/2008
vanishpoint i.v. catheter RETRACTABLE TECHNOLOGIES, INC. K081420 11/07/2008
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