FDA 510(k) Applications Submitted by Reckitt Benckiser LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K151884 | 07/09/2015 | K-Y Marilyn Pleasure Gel | Reckitt Benckiser LLC |
| K143532 | 12/12/2014 | Durex Silicone | Reckitt Benckiser LLC |
| K173504 | 11/13/2017 | K-Y Silicone | Reckitt Benckiser LLC |
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