Male Latex Condom HA
FDA 510(k) clearance K252622 · decided 2026-05-04
Clearance details
- K-number
- K252622
- Device name
- Male Latex Condom HA
- Applicant
- Okamoto USA, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2025-08-19
- Decision date
- 2026-05-04
- Days to decision
- 258 days
- Clearance type
- Abbreviated
- Product code
- HIS
- Device class
- 2
- Regulation number
- 884.5300
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Sandusky, OH, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.