The following data is part of a premarket notification filed by Procter & Gamble Co. with the FDA for Unscented Interlabial Menstrual Pad.
| Device ID | K993870 |
| 510k Number | K993870 |
| Device Name: | UNSCENTED INTERLABIAL MENSTRUAL PAD |
| Classification | Pad, Menstrual, Unscented |
| Applicant | PROCTER & GAMBLE CO. 6100 CENTER HILL AVE. Cincinnati, OH 45224 |
| Contact | Mark M Anderson |
| Correspondent | Mark M Anderson PROCTER & GAMBLE CO. 6100 CENTER HILL AVE. Cincinnati, OH 45224 |
| Product Code | HHD |
| CFR Regulation Number | 884.5435 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-11-15 |
| Decision Date | 2000-01-18 |
| Summary: | summary |