The following data is part of a premarket notification filed by Kimberly-clark Corp. with the FDA for Kotex Lightdays Deodorant Pantiliners.
| Device ID | K862285 |
| 510k Number | K862285 |
| Device Name: | KOTEX LIGHTDAYS DEODORANT PANTILINERS |
| Classification | Pad, Menstrual, Scented |
| Applicant | KIMBERLY-CLARK CORP. 1201 PENNSYLVANIA AVENUE, N.W. SUITE 730 Washington, DC 20004 |
| Contact | Md, Phd |
| Correspondent | Md, Phd KIMBERLY-CLARK CORP. 1201 PENNSYLVANIA AVENUE, N.W. SUITE 730 Washington, DC 20004 |
| Product Code | HHL |
| CFR Regulation Number | 884.5425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-06-16 |
| Decision Date | 1986-07-08 |