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U.S. Department of Health and Human Services

510(k) Premarket Notification

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91 to 100 of 500 Results *
Decision Date To: 07/22/2019
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510(K)
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'quest', 'pelangi' patient exam gloves (latex) PELANGI RUBBER PRODUCTS SDN. BHD. K891272 04/26/1989
'rapid drug screen' 8 panel-low volume AMERICAN BIO MEDICA CORP. K981705 08/27/1998
'rapid drug screen' 9-panel AMERICAN BIO MEDICA CORP. K983770 12/31/1998
'rapid one' - propoxyphene test AMERICAN BIO MEDICA CORP. K030835 05/22/2003
'rapidone'-methadone test AMERICAN BIO MEDICA CORP. K012164 11/20/2001
'rapidtec 4' test AMERICAN BIO MEDICA CORP. K041712 11/03/2004
'rapidtec' 5a multiple dip test AMERICAN BIO MEDICA CORP. K021114 07/23/2002
'rapidtec'-5m-multiple dip test AMERICAN BIO MEDICA CORP. K023869 04/30/2003
'tdxflx analyzer ABBOTT LABORATORIES K904226 10/29/1990
'tensaid' ELECTRO THERAPEUTIC DEVICES, INC. K863567 10/24/1986

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