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Medline DeNovo 4Pro Electrical Stimulation Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201290
510(k) Type
Traditional
Applicant
Medline Industries, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2020
Days to Decision
130 days
Submission Type
Summary

Medline DeNovo 4Pro Electrical Stimulation Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201290
510(k) Type
Traditional
Applicant
Medline Industries, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2020
Days to Decision
130 days
Submission Type
Summary