OKAMOTO CONDOM — Okamoto USA, Inc. (510(k) K952393)
OKAMOTO CONDOM — Okamoto USA, Inc. (510(k) K952393) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: OKAMOTO CONDOM; Applicant: Okamoto USA, Inc.; Clearance track: 510(k).
| Device name | OKAMOTO CONDOM |
|---|---|
| Applicant | Okamoto USA, Inc. |
| Clearance track | 510(k) |
| Submission number | K952393 |
| Decision | Substantially Equivalent |
| Decision date | 1995-08-09 |
| Date received | 1995-05-22 |
| Product code | HIS |
| Device class | 2 |
| Medical specialty | Obstetrics/Gynecology |
| Applicant location | DC, US |
| Source | openFDA device |
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