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510(k) K200299

Device
Curos Jet Disinfecting Cap
Applicant
3M Company
510(k) number
K200299
Product code
QBP  
Decision
Substantially Equivalent (SESE)
Decision date
2020-10-29
Date received
2020-02-06
Regulation
510(k) Premarket Notification
Classification name
Cap, Device Disinfectant
Medical specialty
510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Cory J Hitzman
Address
2510 Conway Ave., Bldg. 275-5nw-06 St. Paul MN US 55144 55144

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code QBP  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K252006OTTO™ Disinfecting CapIcu Medical, Inc.2026-03-27
K251592SteriHub™ Disinfecting Device and Protective Cover1World Vista Medical2026-02-11
K223914ACTIV™ CapCleansite Medical, Inc.2024-04-05
K193190BD PureHub Disinfecting CapBecton, Dickinson and Company2020-11-09
K192382CapKlenZStar Mountain Medical, Inc.2020-04-20
K190918SwabTip Male Disinfectant CapIcu Medical2020-03-06
K142806DualCapCatheter Connections, Inc.2015-05-22
K140657CUROS RED PORT PROTECTORIvera Medical, Inc.2014-12-04
K142399DualCap IV Pole Strips(Disinfectant Caps for Male Luers)Catheter Connections, Inc.2014-11-19
K130975SWABCAP AND SWABFLUSHExcelsior Medical Corp.2013-12-24
K123967CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERSCatheter Connections, Inc.2013-01-22
K123065CATHETER CONNECTIONS DUALCAP SOLOCatheter Connections, Inc.2012-12-14
K121171CUROS TIPIvera Medical, Inc.2012-11-26
K113842CATHETER CONNECTIONS' DUALCAP SOLOCatheter Connections, Inc.2012-01-27
K111992CUROS PORT PROTECTORIvera Medical, Inc.2012-01-12

Legacy Summary#

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FDA Review#

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