The following data is part of a premarket notification filed by Procter & Gamble, Inc. with the FDA for Always Menstrual Pads.
| Device ID | K071827 |
| 510k Number | K071827 |
| Device Name: | ALWAYS MENSTRUAL PADS |
| Classification | Pad, Menstrual, Unscented |
| Applicant | PROCTER & GAMBLE, INC. 6110 CENTER HILL AVENUE Cincinnati, OH 45224 |
| Contact | Lenore Faulhaber |
| Correspondent | Lenore Faulhaber PROCTER & GAMBLE, INC. 6110 CENTER HILL AVENUE 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 | 2007-07-03 |
| Decision Date | 2007-09-20 |
| Summary: | summary |