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Durex Penck III Regular

Page Type
Cleared 510(K)
510(k) Number
K222068
510(k) Type
Traditional
Applicant
Rb Health (Us), LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/2022
Days to Decision
90 days
Submission Type
Summary

Durex Penck III Regular

Page Type
Cleared 510(K)
510(k) Number
K222068
510(k) Type
Traditional
Applicant
Rb Health (Us), LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/2022
Days to Decision
90 days
Submission Type
Summary