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Indiba Diathermia Radiofrequency Device - Activ; Indiba Diathermia Radiofrequency Device - Deep Care

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161458
510(k) Type
Traditional
Applicant
Indiba USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2016
Days to Decision
130 days
Submission Type
Summary

Indiba Diathermia Radiofrequency Device - Activ; Indiba Diathermia Radiofrequency Device - Deep Care

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161458
510(k) Type
Traditional
Applicant
Indiba USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2016
Days to Decision
130 days
Submission Type
Summary