The following data is part of a premarket notification filed by Johnson & Johnson Professionals, Inc. with the FDA for Stayfree* Deodorant Maxi-pads.
| Device ID | K834302 |
| 510k Number | K834302 |
| Device Name: | STAYFREE* DEODORANT MAXI-PADS |
| Classification | Pad, Menstrual, Scented |
| Applicant | JOHNSON & JOHNSON PROFESSIONALS, INC. 325 PARAMOUNT DR. Raynham, MA 02767 -0350 |
| Product Code | HHL |
| CFR Regulation Number | 884.5425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-12-09 |
| Decision Date | 1984-01-17 |