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SJM CONFIRM MODEL DM2100 IMPLANTABLE CARDIAC MONITOR AND MODEL DM2100A PATIENT ACTIVATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081365
510(k) Type
Traditional
Applicant
St Jude Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2008
Days to Decision
92 days
Submission Type
Summary

SJM CONFIRM MODEL DM2100 IMPLANTABLE CARDIAC MONITOR AND MODEL DM2100A PATIENT ACTIVATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081365
510(k) Type
Traditional
Applicant
St Jude Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2008
Days to Decision
92 days
Submission Type
Summary