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U.S. Department of Health and Human Services

510(k) Premarket Notification
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51 to 60 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 03/24/2017
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510(K)
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iv sets CRITIKON COMPANY,LLC K811107 06/12/1981
nitroglycerin i.v. administration set CRITIKON COMPANY,LLC K833939 02/21/1984
rate-mate nitroglycerin i.v. administration set CRITIKON COMPANY,LLC K873729 12/29/1987
micro infusion set DELTEC SYSTEMS, INC. K833949 01/11/1984
accu-chek ultraflex infusion set DISETRONIC MEDICAL SYSTEMS AG K070189 02/21/2007
disetronic rapid subcutaneous infusion set and disteronic rapid d subcutaneous infusion set DISETRONIC MEDICAL SYSTEMS AG K003977 02/15/2001
ultraflex infusion set DISETRONIC MEDICAL SYSTEMS AG K033892 03/09/2004
v set GO MEDICAL INDUSTRIES PTY. LTD. K900336 10/04/1990
lymphangiography set special 30g HYPERION, INC. K834071 01/25/1984
imed technology intravascular administration set, imed technology extension set IMED TECHNOLOGY, INC. K150513 05/28/2015
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