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FDA 510(k) Applications Submitted by DIAGNOSTIC MONITORING SOFTWARE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K062007
07/17/2006
DMS 300-7
DIAGNOSTIC MONITORING SOFTWARE
K062088
07/24/2006
PREMIER 11 HOLTER
DIAGNOSTIC MONITORING SOFTWARE
K133014
09/25/2013
DMS 300-2W HOLTER ECG RECORDER
DIAGNOSTIC MONITORING SOFTWARE
K062959
09/29/2006
DMS 300-2, 300-3 AND 300-4
DIAGNOSTIC MONITORING SOFTWARE
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