Prevantics Device Swab

FDA 510(k) K132380 · Professional Disposables International, Inc.

Substantially Equivalent

510(k) numberK132380

Submission

Device name
Prevantics Device Swab
Applicant
Professional Disposables International, Inc.
Orangeburg, NY, US
Received
July 31, 2013
Decision date
August 27, 2014
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

Other 510(k)s with product code LKB

510(k)DeviceApplicantDecision
K121655BD Alcohol SwabLKB · Traditional Becton, Dickinson & CO03/20/2013SE
K112791Sitescrub Ipa DeviceLKB · Traditional C. R. Bard02/24/2012SE
K912161I.V. Starr KitLKB · Traditional Medical Device Inspection Co., Inc.10/08/1991SE
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

Questions and answers

When was Prevantics Device Swab cleared by the FDA?

Prevantics Device Swab (K132380) received a 510(k) decision of Substantially Equivalent on August 27, 2014, 392 days after the submission was received.

What is the product code of K132380?

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