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U.S. Department of Health and Human Services

510(k) Premarket Notification
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51 to 60 of 490 Results
ProductCode: FOZ Decision Date To: 01/23/2022
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Export all 490 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
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510(K)
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top venula i.v. catheter set TOP SURGICAL MANUFACTURERS CO. K832624 11/21/1983
release of ethylene oxide-steriliz. dev DESERET MEDICAL, INC. K832558 11/28/1983
angio-set intravenous cath. set DESERET MEDICAL, INC. K833657 12/27/1983
centracath #130,135 & 137-hemocath # EXCO, INC. K833079 12/29/1983
injection cap BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC K834480 02/04/1984
deseret neonatal catheter set PARKE-DAVIS CO. K834393 02/13/1984
central vein catherization tray cc-20 PACKAGING TECHNOLOGIES, INC. K834073 02/28/1984
pbc scalp vein set PHILADELPHIA BIOLOGICS CENTER K834255 03/12/1984
deseret central venous catheter PARKE-DAVIS CO. K840862 03/19/1984
deseret multilumen subclavian jugular PARKE-DAVIS CO. K840183 03/19/1984
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