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U.S. Department of Health and Human Services

510(k) Premarket Notification
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121 to 130 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 09/03/2015
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model number: rms1-2604, rms1-2614, rms1-2404, rms1-2414, rms2-2604, rms2-2614, rms2-2404, rms2-2414, rms3-2604, rms3-26 REPRO-MED SYSTEMS, INC. DBA RMS MEDICAL PRODUCTS K122404 05/06/2013
models: 52-01-0, 52-01-1 Y K811110 06/11/1981
modification to 30 extension set CHURCHILL MEDICAL SYSTEMS, INC. K021395 05/13/2002
modification to: liftloc saftey infusion set SPECIALTY HEALTH PRODUCTS, INC. K042234 09/08/2004
mr extension set (001) UNIVERSITY OF MICHIGAN K964968 02/27/1997
multiple i.v. sets C. B. DUMONT COMPANY, INC. K854804 02/12/1986
needlesafe handguard ADRIAN ANESTHESIA SYSTEMS, INC. K931813 07/22/1993
nexiva™ closed iv catheter system with nearport™ iv access Becton Dickinson Infusion Therapy Systems Inc. K231239 09/22/2023
nitroglycerin i.v. administration set CRITIKON COMPANY,LLC K833939 02/21/1984
nitroglycerin infusion set LYPHOMED, INC. K853019 11/12/1985
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