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INTRICON DATRIX SIRONA EVENT/ HOLTER RECORDER

Page Type
Cleared 510(K)
510(k) Number
K112601
510(k) Type
Traditional
Applicant
Intricon Datrix Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2011
Days to Decision
63 days
Submission Type
Summary

INTRICON DATRIX SIRONA EVENT/ HOLTER RECORDER

Page Type
Cleared 510(K)
510(k) Number
K112601
510(k) Type
Traditional
Applicant
Intricon Datrix Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2011
Days to Decision
63 days
Submission Type
Summary