The following data is part of a premarket notification filed by Kimberly-clark Corp. with the FDA for Kotex Security Tube Tampons.
Device ID | K802193 |
510k Number | K802193 |
Device Name: | KOTEX SECURITY TUBE TAMPONS |
Classification | Tampon, Menstrual, Unscented |
Applicant | KIMBERLY-CLARK CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | HEB |
CFR Regulation Number | 884.5470 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1980-09-10 |
Decision Date | 1980-11-12 |