The following data is part of a premarket notification filed by Kimberly-clark Corp. with the FDA for Kotex Profile Shaped Maxi Pad.
| Device ID | K861902 |
| 510k Number | K861902 |
| Device Name: | KOTEX PROFILE SHAPED MAXI PAD |
| Classification | Pad, Menstrual, Unscented |
| Applicant | KIMBERLY-CLARK CORP. 2100 WINCHESTER RD. P.O. BOX 2001 Neenah, WI 54957 -2001 |
| Contact | Bonnie Wan |
| Correspondent | Bonnie Wan KIMBERLY-CLARK CORP. 2100 WINCHESTER RD. P.O. BOX 2001 Neenah, WI 54957 -2001 |
| Product Code | HHD |
| CFR Regulation Number | 884.5435 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-05-16 |
| Decision Date | 1986-06-09 |