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FDA 510(k)

VENTURE WIRE CONTROL CATHETER, MODEL WCC

K-Number: K042910 · 2004-11-22

ApplicantVelocimed, Inc.
Decision Date2004-11-22
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VENTURE WIRE CONTROL CATHETER, MODEL WCC is the device name listed in this FDA 510(k) record. The listed applicant is Velocimed, Inc.. It received FDA 510(k) clearance on 2004-11-22 under 510(k) number K042910. 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 VENTURE WIRE CONTROL CATHETER, MODEL WCC?

VENTURE WIRE CONTROL CATHETER, MODEL WCC is a medical device that received FDA 510(k) clearance on 2004-11-22. The listed applicant is Velocimed, Inc.. The 510(k) number is K042910.

When did VENTURE WIRE CONTROL CATHETER, MODEL WCC receive FDA 510(k) clearance?

VENTURE WIRE CONTROL CATHETER, MODEL WCC received FDA 510(k) clearance on 2004-11-22, under 510(k) number K042910.

Who is the listed applicant for VENTURE WIRE CONTROL CATHETER, MODEL WCC?

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

What is the FDA product code for VENTURE WIRE CONTROL CATHETER, MODEL WCC?

The FDA product code for VENTURE WIRE CONTROL CATHETER, MODEL WCC is DQY.

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 Velocimed, 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.

K052523PROXIS SYSTEMK043084PREMERE DELIVERY SHEATH, MODEL PDSK042117PROXIS SYSTEM, MODEL EPS 101K040922VENTURE WIRE CONTROL CATHETER

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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