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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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Device Name
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510(K)
Number
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catheter-thru-needle device ABBOTT LABORATORIES K770403 03/16/1977
catheter with guidewire assembly device ABBOTT LABORATORIES K900056 08/15/1990
0.9% sodium chloride diluent in plastic syringe ABBOTT LABORATORIES K953805 06/28/1996
cvp polyurethane catheter ABBOTT LABORATORIES K961552 02/10/1997
polycath-h catheter ABBOTT LABORATORIES K854308 04/07/1986
modification to syringe prefilled with 0.9% sodium chloride ABBOTT LABORATORIES K001616 07/27/2000
needle connecting set, blunt ABBOTT LABORATORIES K780105 02/21/1978
winged catheter ABBOTT LABORATORIES K830765 03/31/1983
intravenous catheter placement unit & ACCESS DEVICES, INC. K823017 11/01/1982
hydromid Access Vascular Inc. K203069 02/08/2021
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