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FDA 510(k)

CATHETER CONNECTIONS' DUALCAP DUO

K-Number: K112985 · 2011-11-09

Decision Date2011-11-09
Product CodeQBP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATHETER CONNECTIONS' DUALCAP DUO 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 2011-11-09 under 510(k) number K112985. 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 DUO?

CATHETER CONNECTIONS' DUALCAP DUO is a medical device that received FDA 510(k) clearance on 2011-11-09. The listed applicant is Catheter Connections, Inc.. The 510(k) number is K112985.

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

CATHETER CONNECTIONS' DUALCAP DUO received FDA 510(k) clearance on 2011-11-09, under 510(k) number K112985.

Who is the listed applicant for CATHETER CONNECTIONS' DUALCAP DUO?

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 DUO?

The FDA product code for CATHETER CONNECTIONS' DUALCAP DUO 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.

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.

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.

Official Source

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

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