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Cure Ultra Male, Cure Ultra Female, Cure Ultra Plus

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221593
510(k) Type
Traditional
Applicant
ConvaTec, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2022
Days to Decision
168 days
Submission Type
Summary

Cure Ultra Male, Cure Ultra Female, Cure Ultra Plus

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221593
510(k) Type
Traditional
Applicant
ConvaTec, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2022
Days to Decision
168 days
Submission Type
Summary