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U.S. Department of Health and Human Services

510(k) Premarket Notification
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31 to 40 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 08/29/2016
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Device Name
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510(K)
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model 72-81-0 unvented solution adm. set Y K801613 08/12/1980
model 86-01-1 260 solution admin. set Y K801872 08/27/1980
model 86-21-0 260 secondary medication Y K801873 08/27/1980
model 86-21-1 260 approx. 60 drops/ventd Y K801874 08/27/1980
models: 52-01-0, 52-01-1 Y K811110 06/11/1981
primary solution admin. set-#86-01-0 260 Y K801871 08/27/1980
universal vented & non/volume infus- Y K833034 11/07/1983
infusion sets with precision filter for single use, precision infusion filter for single use, extended infusion sets for single use Wuhan W.E.O Science & Technology Development Co., Ltd. K181870 02/26/2019
extension set WESTMARK, STERILE PACKING SYSTEMS, INC. (SPS) K896561 02/01/1990
wall iv extension tube WALLA MEDICAL SYSTEMS, INC. K940689 03/22/1994
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