Catheter Connections Dualcap Solo

FDA 510(k) K123065 · Catheter Connections, Inc.

Substantially Equivalent

510(k) numberK123065

Submission

Device name
Catheter Connections Dualcap Solo
Applicant
Catheter Connections, Inc.
Salt Lake City, UT, US
Received
October 1, 2012
Decision date
December 14, 2012
Decision
Substantially Equivalent (SESE)
Type
Special 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

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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

More from Catheter Connections, Inc.

510(k)DeviceDecision
K142806DualCapQBP · Traditional 05/22/2015SE
K142399DualCap IV Pole Strips(Disinfectant Caps for Male Luers)QBP · Traditional 11/19/2014SE
K123967Catheter Connections' Dark Blue Dualcap for Male LuersQBP · Special 01/22/2013SE
K113842Catheter Connections' Dualcap SoloQBP · Special 01/27/2012SE
K112985Catheter Connections' Dualcap DuoQBP · Special 11/09/2011SE
K093229Catheter Connections DualcapQBP · Traditional 04/08/2010SE

Questions and answers

When was Catheter Connections Dualcap Solo cleared by the FDA?

Catheter Connections Dualcap Solo (K123065) received a 510(k) decision of Substantially Equivalent on December 14, 2012, 74 days after the submission was received.

What is the product code of K123065?

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