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U.S. Department of Health and Human Services

510(k) Premarket Notification
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61 to 70 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 09/26/2016
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510(K)
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mr extension set (001) UNIVERSITY OF MICHIGAN K964968 02/27/1997
modification to: liftloc saftey infusion set SPECIALTY HEALTH PRODUCTS, INC. K042234 09/08/2004
modification to 30 extension set CHURCHILL MEDICAL SYSTEMS, INC. K021395 05/13/2002
models: 52-01-0, 52-01-1 Y K811110 06/11/1981
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
model iv 1500 standard burette VALLEYLAB, INC. K781637 12/12/1978
model 86-21-1 260 approx. 60 drops/ventd Y K801874 08/27/1980
model 86-21-0 260 secondary medication Y K801873 08/27/1980
model 86-01-1 260 solution admin. set Y K801872 08/27/1980
model 72-81-0 unvented solution adm. set Y K801613 08/12/1980
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