Connector Components with Balance Biosurface

FDA 510(k) K122811 · Medtronic, Inc.

Substantially Equivalent

510(k) numberK122811

Submission

Device name
Connector Components with Balance Biosurface
Applicant
Medtronic, Inc.
Minneapolis, MN, US
Received
September 13, 2012
Decision date
October 12, 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
DTL – Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4290
Specialty
Cardiovascular

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K152528Attachable Cath Lab Hemostasis ValveDTL · Traditional Galt Medical Corp.12/02/2015SE
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K140475Rotating AdaptersDTL · Traditional Merit Medical Systems, Inc.04/16/2014SE
K131124ColignDTL · Traditional Jilin Coronado Medical , Ltd.08/28/2013SE
K123448Affinity Flexible Luer Lock Adapter with Balance Biosurface, Affinity Flexible Luer Lock…DTL · Special Medtronic, Inc.12/13/2012SE
K122301Guardian II Hemostasis Valve Guardian II NC Hemostasis ValveDTL · Traditional Vascular Solutions Zerusa , Ltd.09/07/2012SE
K120069Medline Stopcock and ManifoldDTL · Traditional Medline Industries, Inc.04/03/2012SE
K113148E-PassDTL · Traditional Synexmed(Shenzhen)Company Limited02/28/2012SE
K113845Tubing, Conmnectors, and Accessories Wit Balance BiosurfaceDTL · Special Medtronic, Inc.01/25/2012SE
K113132Disposable Hemostatic Y-ConnectorsDTL · Traditional Coeur, Inc.01/20/2012SE

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Questions and answers

When was Connector Components with Balance Biosurface cleared by the FDA?

Connector Components with Balance Biosurface (K122811) received a 510(k) decision of Substantially Equivalent on October 12, 2012, 29 days after the submission was received.

What is the product code of K122811?

The FDA product code is DTL – Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4290.