KOTEX(R) SECUREHOLD SUPER CURVE/CURVED MAXI PADS— 510(k) K925250

Name: FDA 510(k) clearance K925250
Creator: U.S. Food and Drug Administration
Published: 1993-03-03

Substantially Equivalent

Kimberly-Clark Corp.

FDA 510(k) clearance K925250 for KOTEX(R) SECUREHOLD SUPER CURVE/CURVED MAXI PADS, Substantially Equivalent on 1993-03-03. Applicant: Kimberly-Clark Corp.. Device class: 1.

Clearance details

Applicant: Kimberly-Clark Corp.
Product code: Code HHD
Device class: Class 1
Regulation: 21 CFR 884.5435
Advisory panel: Obstetrics/Gynecology
Date received: 1992-10-16
Decision date: 1993-03-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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