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Durex Penck Standard, Durex Penck XL

Page Type
Cleared 510(K)
510(k) Number
K200672
510(k) Type
Traditional
Applicant
RB Health (US) LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2020
Days to Decision
238 days
Submission Type
Summary

Durex Penck Standard, Durex Penck XL

Page Type
Cleared 510(K)
510(k) Number
K200672
510(k) Type
Traditional
Applicant
RB Health (US) LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2020
Days to Decision
238 days
Submission Type
Summary