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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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