The following data is part of a premarket notification filed by Procter & Gamble Mfg. Co. with the FDA for Scented Menstrual Pad.
| Device ID | K834131 |
| 510k Number | K834131 |
| Device Name: | SCENTED MENSTRUAL PAD |
| Classification | Pad, Menstrual, Scented |
| Applicant | PROCTER & GAMBLE MFG. CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | HHL |
| CFR Regulation Number | 884.5425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-12-01 |
| Decision Date | 1983-12-29 |