K203536 is an FDA 510(k) clearance for the Male Latex Condom. This device is classified as a Condom (Class II - Special Controls, product code HIS).
Submitted by Global Protection Corp. (Boston, US). The FDA issued a Cleared decision on September 3, 2021, 274 days after receiving the submission on December 3, 2020.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.5300.
| 510(k) Number | K203536 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 03, 2020 |
| Decision Date | September 03, 2021 |
| Days to Decision | 274 days |
| Submission Type | Abbreviated |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Statement |
| Product Code | HIS - Condom |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.5300 |