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H3+ Holter Recorder

Page Type
Cleared 510(K)
510(k) Number
K152626
510(k) Type
Traditional
Applicant
Mortara Instrument, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2016
Days to Decision
164 days
Submission Type
Summary

H3+ Holter Recorder

Page Type
Cleared 510(K)
510(k) Number
K152626
510(k) Type
Traditional
Applicant
Mortara Instrument, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2016
Days to Decision
164 days
Submission Type
Summary