FDA 510(k) Applications Submitted by LELO Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160644 | 03/07/2016 | Lelo Hex Natural Rubber Latex Condom | LELO Inc. |
| K162511 | 09/08/2016 | LELO RESPECT HEX Natural Rubber Latex Condom | LELO INC. |
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