The following data is part of a premarket notification filed by Kimberly-clark Corp. with the FDA for Kotex Maxi Pads.
| Device ID | K850033 |
| 510k Number | K850033 |
| Device Name: | KOTEX MAXI PADS |
| Classification | Pad, Menstrual, Unscented |
| Applicant | KIMBERLY-CLARK CORP. 1201 PENNSYLVANIA AVENUE, N.W. SUITE 730 Washington, DC 20004 |
| Contact | Bonnie B Wan |
| Correspondent | Bonnie B Wan KIMBERLY-CLARK CORP. 1201 PENNSYLVANIA AVENUE, N.W. SUITE 730 Washington, DC 20004 |
| Product Code | HHD |
| CFR Regulation Number | 884.5435 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-01-03 |
| Decision Date | 1985-03-01 |