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DERMASENSE PLUS DISPERSIVE ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K980171
510(k) Type
Traditional
Applicant
HORIZON MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1998
Days to Decision
38 days
Submission Type
Summary

DERMASENSE PLUS DISPERSIVE ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K980171
510(k) Type
Traditional
Applicant
HORIZON MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1998
Days to Decision
38 days
Submission Type
Summary