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DERMASENSE PLUS DISPERSIVE ELECTRODE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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