FDA 510(k) Applications Submitted by REPROCESSING PRODUCTS CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K123805 12/11/2012 E-Z CHEK BLOOD LEAK TEST STRIPS REPROCESSING PRODUCTS CORP.
K090338 02/10/2009 ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE REPROCESSING PRODUCTS CORP.
K101750 06/22/2010 RPC E-Z CHEK 6.8-8.5 PH TEST STRIPS, MODEL K100-0117 AND E-Z CHEK 0-14 PH TEST STRIPS, MODEL K100-0104 REPROCESSING PRODUCTS CORP.
K974064 10/27/1997 MICRO X RESIDUAL TEST STRIPS REPROCESSING PRODUCTS CORP.
K974426 10/27/1997 POTENCY TEST STRIPS, INDICATOR TEST STRIPS REPROCESSING PRODUCTS CORP.


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