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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 493 Results
ProductCode: FOZ Decision Date To: 01/23/2022
 
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510(K)
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catheter, intravascular (medicut t) SHERWOOD MEDICAL INDUSTRIES K760163 07/20/1976
kit, catheter JELCO LABORATORIES K760319 08/11/1976
cannula, intravenous, heparinized SHERWOOD MEDICAL INDUSTRIES K770511 04/29/1977
iv catheter hub JELCO LABORATORIES K771381 10/13/1977
cannula, intravenous, teflon SHERWOOD MEDICAL INDUSTRIES K770510 05/10/1977
i.v. catheter NDM CORP. K772354 01/31/1978
catheters, over-the-needle CUTTER LABORATORIES, INC. K770751 05/26/1977
duo-cath femoral MEDICAL DEVICE LABORATORIES K771573 09/15/1977
i.v. catheter placement unit AMERICAN VIGGO K770181 03/30/1977
catheter-thru-needle device ABBOTT LABORATORIES K770403 03/16/1977
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