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CPR Dura-Padz Reusable Defibrillation Electrode with Dura-padz Gel

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150198
510(k) Type
Traditional
Applicant
Bio-Detek, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2015
Days to Decision
93 days
Submission Type
Summary

CPR Dura-Padz Reusable Defibrillation Electrode with Dura-padz Gel

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150198
510(k) Type
Traditional
Applicant
Bio-Detek, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2015
Days to Decision
93 days
Submission Type
Summary