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U.S. Department of Health and Human Services

510(K) Premarket Notification
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Device Name
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Applicant
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510(K)
Number
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Decision
Date
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vomed urethra olive, models 1420 000, 1425 000, 1430 000 VOMED VOLZER MEDIZINTECHNIK GMBH & CO. k023019 12/10/2002
wako apolipoprotein high level calibrator WAKO CHEMICALS, USA, INC. k001004 06/01/2000
wako autokit lp(a) & lp(a) calibrator/aeroset WAKO CHEMICALS, USA, INC. k001931 07/24/2000
wako autokit lp(a) & lp(a) calibrator/beckman cx WAKO CHEMICALS, USA, INC. k001934 07/24/2000
wako autokit lp(a) & lp(a) calibrator/cobas bio WAKO CHEMICALS, USA, INC. k001933 07/24/2000
wako autokit lp(a) and lp(a) calibrator/cobas fara WAKO CHEMICALS, USA, INC. k001929 07/24/2000
wako autokit lp(a)/ ra,500/1000, WAKO CHEMICALS, USA, INC. k001920 07/23/2000
wako autokit lp(a)/dade demension WAKO CHEMICALS, USA, INC. k001919 07/23/2000
wako autokit lp(a)/express 550 WAKO CHEMICALS, USA, INC. k001921 07/23/2000
wako hdl-c/ldl-c calibrator WAKO CHEMICALS, USA, INC. k001005 06/01/2000

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
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