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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