K875111 is an FDA 510(k) clearance for the RUBBER CONTRACEPTIVE, LATEX CONDOMS. This device is classified as a Condom (Class II - Special Controls, product code HIS).
Submitted by Okamoto USA, Inc. (Stratford, US). The FDA issued a Cleared decision on February 26, 1988, 74 days after receiving the submission on December 14, 1987.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.5300.
| 510(k) Number | K875111 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 14, 1987 |
| Decision Date | February 26, 1988 |
| Days to Decision | 74 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | - |
| Product Code | HIS - Condom |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.5300 |