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FDA 510(k)

CATHETER CONNECTIONS DUALCAP

K-Number: K093229 · 2010-04-08

ApplicantCatheter Connections, Inc.
Decision Date2010-04-08
Product CodeQBP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATHETER CONNECTIONS DUALCAP is the device name listed in this FDA 510(k) record. The listed applicant is Catheter Connections, Inc.. It received FDA 510(k) clearance on 2010-04-08 under 510(k) number K093229. The device is classified under product code QBP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER CONNECTIONS DUALCAP?

CATHETER CONNECTIONS DUALCAP is a medical device that received FDA 510(k) clearance on 2010-04-08. The listed applicant is Catheter Connections, Inc.. The 510(k) number is K093229.

When did CATHETER CONNECTIONS DUALCAP receive FDA 510(k) clearance?

CATHETER CONNECTIONS DUALCAP received FDA 510(k) clearance on 2010-04-08, under 510(k) number K093229.

Who is the listed applicant for CATHETER CONNECTIONS DUALCAP?

The FDA 510(k) record lists Catheter Connections, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATHETER CONNECTIONS DUALCAP?

The FDA product code for CATHETER CONNECTIONS DUALCAP is QBP.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Catheter Connections, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K123967CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERSK123065CATHETER CONNECTIONS DUALCAP SOLOK113842CATHETER CONNECTIONS' DUALCAP SOLOK112985CATHETER CONNECTIONS' DUALCAP DUO

Related Devices (Code: QBP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252006OTTO™ Disinfecting CapIcu Medical, Inc.K251592SteriHub™ Disinfecting Device and Protective Cover1World Vista MedicalK223914ACTIV™ CapCleansite Medical, Inc.K193190BD PureHub Disinfecting CapBecton, Dickinson and CompanyK200299Curos Jet Disinfecting Cap3M CompanyK192382CapKlenZStar Mountain Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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