510(k) K924502
K924502 is an FDA 510(k) premarket notification submitted by Keema And Co. for the device "REUSABLE MENSTRUAL PAD". The FDA issued a decision of Substantially Equivalent on Nov 30, 1994. The device falls under product code HHD (Pad, Menstrual, Unscented), a Class I device regulated under 21 CFR 884.5435.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 30, 1994
- Date Received
- Sep 4, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Pad, Menstrual, Unscented
- Device Class
- Class I
- Regulation Number
- 884.5435
- Review Panel
- OB
- Submission Type
- 510(k) Exempt
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.