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U.S. Department of Health and Human Services

510(k) Premarket Notification
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41 to 50 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 09/26/2016
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510(K)
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safety injection port, modification RIVERSIDE TECHNOLOGY, INC. K913311 09/13/1991
safety blood collection / infusion set (with/without needle holder), blood collection / infusion set (with/without needle holder) Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd. K214075 04/12/2022
safelock disposable blood collection set, disposable blood collection set JIANGYIN CAINA TECHNOLOGY CO., LTD. K151991 12/11/2015
saf-t clik i.v. in-line connector & extension set RYAN MEDICAL, INC. K901729 06/18/1990
rms subcutaneous needle set REPRO-MED SYSTEMS, INC. K102512 05/20/2011
rate-mate nitroglycerin i.v. administration set CRITIKON COMPANY,LLC K873729 12/29/1987
prn adapter BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC K933467 12/12/1994
primary solution set with universal spike, injection site and male luer lock CHURCHILL MEDICAL SYSTEMS, INC. K011336 06/12/2001
primary solution admin. set-#86-01-0 260 Y K801871 08/27/1980
pressure activated check valve CHURCHILL MEDICAL SYSTEMS, INC. K011888 09/10/2001
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