K952393 is an FDA 510(k) clearance for the OKAMOTO CONDOM. This device is classified as a Condom (Class II - Special Controls, product code HIS).
Submitted by Okamoto USA, Inc. (Washington, US). The FDA issued a Cleared decision on August 9, 1995, 79 days after receiving the submission on May 22, 1995.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.5300.
| 510(k) Number | K952393 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 22, 1995 |
| Decision Date | August 09, 1995 |
| Days to Decision | 79 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | HIS — Condom |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.5300 |