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Revive Reusable Bladder Support

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183468
510(k) Type
Traditional
Applicant
Rinovum Subsidiary 2, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2019
Days to Decision
42 days
Submission Type
Summary

Revive Reusable Bladder Support

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183468
510(k) Type
Traditional
Applicant
Rinovum Subsidiary 2, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2019
Days to Decision
42 days
Submission Type
Summary