FDA 510(k) Applications Submitted by SCOTTCARE CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K081359 05/15/2008 GENESIS ECP SCOTTCARE CORPORATION
K142180 08/08/2014 TELESENSE SCOTTCARE CORPORATION
K092947 09/24/2009 TELESENTRY, MODEL TS01 SCOTTCARE CORPORATION
K083382 11/14/2008 CHROMA, MODEL: RZ153C SCOTTCARE CORPORATION


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