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

Male Latex Condom HA

K Number: K252622 · Decision May 4, 2026
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
400
Applicant Total
15
Review Days
258

Basic Information

Device Name
Male Latex Condom HA
K Number
K252622
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
884.5300
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Okamoto USA, Inc.
Date Received
August 19, 2025
Decision Date
May 4, 2026
Product Code
HIS
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
HIS Condom

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