FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Okamoto 002 Lubricated Polyurethane Male Condom

K Number: K203541 · Decision Feb 25, 2022
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
22
Applicant Total
15
Review Days
449

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Basic Information

Device Name
Okamoto 002 Lubricated Polyurethane Male Condom
K Number
K203541
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5300
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Okamoto USA, Inc.
Date Received
December 3, 2020
Decision Date
February 25, 2022
Product Code
MOL
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MOL Condom, Synthetic

Similar 510(k) Clearances

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Other Clearances by Okamoto USA, Inc.

K Number Device Name
K252622 Male Latex Condom HA
K243584 0.04 ZERO ZERO FOUR Male Latex Condom
K192669 Extremely Thin 003, ZERO ZERO THREE
K141256 OKAMOTO STUDDED CONDOM
K140379 MEGA BIG BOY CONDOM
K090259 OKAMOTO ULTRA THIN
K952393 OKAMOTO CONDOM
K902804 EXTEND STABILITY DATE FOR CONDOM W/SPERM LUBRICANT
K896339 MODIFIED LABELING ON OKAMOTO HARMONY CONDOM
K884402 EXTRA STRENGTH SKIN LESS SKIN CONDOM
Search all 15 clearances from Okamoto USA, Inc. →