The following data is part of a premarket notification filed by Procter & Gamble Mfg. Co. with the FDA for Always Super Maxipad-unscented.
| Device ID | K850940 |
| 510k Number | K850940 |
| Device Name: | ALWAYS SUPER MAXIPAD-UNSCENTED |
| Classification | Pad, Menstrual, Unscented |
| Applicant | PROCTER & GAMBLE MFG. CO. P.O. BOX 599 Cincinnati, OH 45201 |
| Contact | James T O'reilly |
| Correspondent | James T O'reilly PROCTER & GAMBLE MFG. CO. P.O. BOX 599 Cincinnati, OH 45201 |
| Product Code | HHD |
| CFR Regulation Number | 884.5435 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-03-07 |
| Decision Date | 1985-05-14 |