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FDA 510(k) Applications Submitted by HOWARD SMITH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100266
01/29/2010
ACTIWAVE 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, ACTIWAVE CARDIO MODEL 08-514, 08-521, 08-536, 08-557, 08-603
CAMNTECH, LTD
K132764
09/04/2013
MOTION WATCH AND PRO-DIARY
CAMNTECH, LTD
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