Sitescrub Ipa Device

FDA 510(k) K112791 · C. R. Bard

Substantially Equivalent

510(k) numberK112791

Submission

Device name
Sitescrub Ipa Device
Applicant
C. R. Bard
Salt Lake Ciy,, UT, US
Received
September 26, 2011
Decision date
February 24, 2012
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LKB – Pad, Alcohol, Device Disinfectant
Device class
Unclassified

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K912731Steri-SwabLKB · Traditional Westlock Investments (Usa), Inc.10/02/1991SE
K910735Hexidis Alcohol SwabLKB · Traditional Specialites Septodont04/02/1991SE
K896898Bowen Electrode Skin Prepatory CleanserLKB · Traditional Bowen & Company, Inc.04/04/1990SE
K896835Alcohol Prep and Povidone-Iodine PrepLKB · Traditional Norpak Mfg., Inc.01/11/1990SE
K894791Baxter Acetone-Alcohol Swabstick, SterileLKB · Traditional Span-America Medical Systems, Inc.10/03/1989SE
K893958Baxter Acetone-Alcohol Prep Pads, SterileLKB · Traditional Span-America Medical Systems, Inc.10/03/1989SE
K892193Quickpad (Alcohol Swabs)LKB · Traditional Holtsch Co., Inc.08/04/1989SE

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Questions and answers

When was Sitescrub Ipa Device cleared by the FDA?

Sitescrub Ipa Device (K112791) received a 510(k) decision of Substantially Equivalent on February 24, 2012, 151 days after the submission was received.

What is the product code of K112791?

The FDA product code is LKB – Pad, Alcohol, Device Disinfectant, a Unclassified device.