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FREMAP ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K152769
510(k) Type
Traditional
Applicant
AD-TECH MEDICAL INSTRUMENT CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2016
Days to Decision
224 days
Submission Type
Summary

FREMAP ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K152769
510(k) Type
Traditional
Applicant
AD-TECH MEDICAL INSTRUMENT CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2016
Days to Decision
224 days
Submission Type
Summary