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Cure Ultra Male, Cure Ultra Female, Cure Ultra Plus

Page Type
Cleared 510(K)
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)
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