Alcohol Pad

FDA 510(k) K080466 · 122 Corporation

Substantially Equivalent

510(k) numberK080466

Submission

Device name
Alcohol Pad
Applicant
122 Corporation
San Diego, CA, US
Received
February 21, 2008
Decision date
October 21, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
QBP – Cap, Device Disinfectant
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

Disinfect needleless access valves and may act as a physical barrier to contamination if not removed for a set period of time

Other 510(k)s with product code QBP

510(k)DeviceApplicantDecision
K252006OTTO™ Disinfecting CapQBP · Traditional Icu Medical, Inc.03/27/2026SE
K251592SteriHub™ Disinfecting Device and Protective CoverQBP · Traditional 1World Vista Medical02/11/2026SE
K223914ACTIV™ CapQBP · Traditional Cleansite Medical, Inc.04/05/2024SE
K193190BD PureHub Disinfecting CapQBP · Traditional Becton, Dickinson and Company11/09/2020SE
K200299Curos Jet Disinfecting CapQBP · Traditional 3M Company10/29/2020SE
K192382CapKlenZQBP · Traditional Star Mountain Medical, Inc.04/20/2020SE
K190918SwabTip Male Disinfectant CapQBP · Traditional Icu Medical03/06/2020SE
K142806DualCapQBP · Traditional Catheter Connections, Inc.05/22/2015SE
K140657Curos Red Port ProtectorQBP · Traditional Ivera Medical, Inc.12/04/2014SE
K142399DualCap IV Pole Strips(Disinfectant Caps for Male Luers)QBP · Traditional Catheter Connections, Inc.11/19/2014SE

Questions and answers

When was Alcohol Pad cleared by the FDA?

Alcohol Pad (K080466) received a 510(k) decision of Substantially Equivalent on October 21, 2008, 243 days after the submission was received.

What is the product code of K080466?

The FDA product code is QBP – Cap, Device Disinfectant, a Class II (moderate risk) device regulated under 21 CFR 880.5440.