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U.S. Department of Health and Human Services

510(k) Premarket Notification

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1 to 10 of 19 Results
ProductCode: FPA Applicant: IMED CORP Decision Date To: 11/24/2014
 
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Export all 19 Records to ExcelExport to Excel | Download Files | More About 510(k)
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510(K)
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vented/nonvented gemini administration s imed corp. K950153 08/24/1995
administration sets with ball float imed corp. K951922 07/19/1995
the imed orion infusion pump and adminis imed corp. K950419 06/21/1995
vented/non-vented gemini administration imed corp. K944320 02/14/1995
versasae plastic cannula- 11 gauge imed corp. K945070 01/13/1995
primary admin set w/univ sp-man below/ab imed corp. K931173 04/15/1994
shrouded needle devices imed corp. K924718 06/18/1993
imed gemini 12 nonvented y-type blood/so imed corp. K894842 09/12/1989
universal disposable infusion set (code jufrey multimed corp. K861518 05/27/1986
universal disposable infusion set (code jufrey multimed corp. K861519 05/27/1986
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