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FDA 510(k) Applications Submitted by Okamoto U.S.A., Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090259
02/02/2009
OKAMOTO ULTRA THIN
OKAMOTO U.S.A., INC.
K140379
02/14/2014
MEGA BIG BOY CONDOM
OKAMOTO U.S.A., INC.
K141256
05/14/2014
OKAMOTO STUDDED CONDOM
OKAMOTO U.S.A., INC.
K192669
09/25/2019
Extremely Thin 003, ZERO ZERO THREE
Okamoto U.S.A., Inc.
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