The following data is part of a premarket notification filed by Kimberly-clark Corp. with the FDA for Kotex Lightdays Deodorant Pantiliners.
| Device ID | K802277 |
| 510k Number | K802277 |
| Device Name: | KOTEX LIGHTDAYS DEODORANT PANTILINERS |
| Classification | Pad, Menstrual, Scented |
| Applicant | KIMBERLY-CLARK CORP. 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 | 1980-09-18 |
| Decision Date | 1980-10-10 |