KOTEX SUPER MAXI PADS— 510(k) K890013

Substantially Equivalent

Kimberly-Clark Corp.

FDA 510(k) clearance K890013 for KOTEX SUPER MAXI PADS, Substantially Equivalent on 1989-04-25. Applicant: Kimberly-Clark Corp.. Device class: 2.

Clearance details

Applicant: Kimberly-Clark Corp.
Product code: Code HHT
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1989-01-03
Decision date: 1989-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.