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DIO IMPLANT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070570
510(k) Type
Traditional
Applicant
Dio Department Dsi, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2008
Days to Decision
412 days
Submission Type
Summary

DIO IMPLANT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070570
510(k) Type
Traditional
Applicant
Dio Department Dsi, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2008
Days to Decision
412 days
Submission Type
Summary