K223883 is an FDA 510(k) clearance for the Daye Tampon. This device is classified as a Tampon, Menstrual, Unscented (Class II - Special Controls, product code HEB).
Submitted by Annes Daye, Ltd. (London, GB). The FDA issued a Cleared decision on August 18, 2023, 234 days after receiving the submission on December 27, 2022.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.5470. An Unscented Menstrual Tampon Is A Plug Made Of Cellulosic Or Synthetic Material That Is Inserted Into The Vagina And Used To Absorb Menstrual Fluid Or Other Vaginal Discharge..
| 510(k) Number | K223883 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 27, 2022 |
| Decision Date | August 18, 2023 |
| Days to Decision | 234 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | HEB - Tampon, Menstrual, Unscented |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.5470 |
| Definition | An Unscented Menstrual Tampon Is A Plug Made Of Cellulosic Or Synthetic Material That Is Inserted Into The Vagina And Used To Absorb Menstrual Fluid Or Other Vaginal Discharge. |