KIMBERLY-CLARK SURGICAL DRAPES WITH AAMI LIQUID BARRIER LEVEL 4 CLAIM— 510(k) K102666

Name: FDA 510(k) clearance K102666
Creator: U.S. Food and Drug Administration
Published: 2010-11-09

Substantially Equivalent

Kimberly-Clark Corp.

FDA 510(k) clearance K102666 for KIMBERLY-CLARK SURGICAL DRAPES WITH AAMI LIQUID BARRIER LEVEL 4 CLAIM, Substantially Equivalent on 2010-11-09. Applicant: Kimberly-Clark Corp.. Device class: 2.

Clearance details

Applicant: Kimberly-Clark Corp.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 2010-09-15
Decision date: 2010-11-09
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Roswell, GA, 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.