The following data is part of a premarket notification filed by Personal Products Co. with the FDA for Stayfree Maxi Pads.
| Device ID | K761233 |
| 510k Number | K761233 |
| Device Name: | STAYFREE MAXI PADS |
| Classification | Pad, Menstrual, Scented |
| Applicant | PERSONAL PRODUCTS CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HHL |
| CFR Regulation Number | 884.5425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-12-10 |
| Decision Date | 1976-12-17 |