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FDA 510(k) Applications Submitted by Kyle Prince
FDA 510(k) Number
Submission Date
Device Name
Applicant
K200672
03/13/2020
Durex Penck Standard, Durex Penck XL
RB Health (US) LLC
K211152
04/19/2021
Durex Condom with Benzocaine
RB Health (US) LLC
K222068
07/14/2022
Durex Penck III Regular
RB Health (US) LLC
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