FOOTHILLS SURGICAL DRAPES— 510(k) K041224

Name: FDA 510(k) clearance K041224
Creator: U.S. Food and Drug Administration
Published: 2005-02-03

Substantially Equivalent

Foothills Industries, Inc.

FDA 510(k) clearance K041224 for FOOTHILLS SURGICAL DRAPES, Substantially Equivalent on 2005-02-03. Applicant: Foothills Industries, Inc.. Device class: 2.

Clearance details

Applicant: Foothills Industries, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 2004-05-10
Decision date: 2005-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marion, NC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KKX

view all

K230645 — BeneHold Surgical Incise Drape with CHG antimicrobial II2023-10-25
K222578 — 3M Ioban CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)2023-05-18
K202208 — BeneHold Surgical Incise Drape with CHG antimicrobial2021-07-30
K200238 — ControlRad Sterile Cover2020-04-26
K163556 — MediClear PreOp2017-09-14

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