K812577 is an FDA 510(k) clearance for the UNSCENTED MENSTRUAL PADS. This device is classified as a Pad, Menstrual, Unscented (Class I - General Controls, product code HHD).
Submitted by Weyerhaeuser Co. (Mchenry, US). The FDA issued a Cleared decision on October 19, 1981, 40 days after receiving the submission on September 9, 1981.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.5435. An Unscented Menstrual Pad Which Is Used To Absorb Menstrual Fluid Or Other Vaginal Discharge And Is Made Of Common Cellulosic And Synthetic Material With An Established Safety Profile..
| 510(k) Number | K812577 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 09, 1981 |
| Decision Date | October 19, 1981 |
| Days to Decision | 40 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | — |
| Product Code | HHD — Pad, Menstrual, Unscented |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 884.5435 |
| Definition | An Unscented Menstrual Pad Which Is Used To Absorb Menstrual Fluid Or Other Vaginal Discharge And Is Made Of Common Cellulosic And Synthetic Material With An Established Safety Profile. |