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FDA 510(k)

VASCULAR SOLUTIONS TWIN-PASS DUAL ACCESS CATHETER

K-Number: K052257 · 2005-11-23

ApplicantVascular Solutions, Inc.
Decision Date2005-11-23
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASCULAR SOLUTIONS TWIN-PASS DUAL ACCESS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Solutions, Inc.. It received FDA 510(k) clearance on 2005-11-23 under 510(k) number K052257. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCULAR SOLUTIONS TWIN-PASS DUAL ACCESS CATHETER?

VASCULAR SOLUTIONS TWIN-PASS DUAL ACCESS CATHETER is a medical device that received FDA 510(k) clearance on 2005-11-23. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K052257.

When did VASCULAR SOLUTIONS TWIN-PASS DUAL ACCESS CATHETER receive FDA 510(k) clearance?

VASCULAR SOLUTIONS TWIN-PASS DUAL ACCESS CATHETER received FDA 510(k) clearance on 2005-11-23, under 510(k) number K052257.

Who is the listed applicant for VASCULAR SOLUTIONS TWIN-PASS DUAL ACCESS CATHETER?

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

What is the FDA product code for VASCULAR SOLUTIONS TWIN-PASS DUAL ACCESS CATHETER?

The FDA product code for VASCULAR SOLUTIONS TWIN-PASS DUAL ACCESS CATHETER is DQY.

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Other records listing Vascular Solutions, Inc. as applicant

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Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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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