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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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