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FDA 510(k)

MODIFICATION TO SUPERCROSS CATHETER

K-Number: K014118 · 2002-01-11

ApplicantAbbott Vascular, Inc.
Decision Date2002-01-11
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO SUPERCROSS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Vascular, Inc.. It received FDA 510(k) clearance on 2002-01-11 under 510(k) number K014118. 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 MODIFICATION TO SUPERCROSS CATHETER?

MODIFICATION TO SUPERCROSS CATHETER is a medical device that received FDA 510(k) clearance on 2002-01-11. The listed applicant is Abbott Vascular, Inc.. The 510(k) number is K014118.

When did MODIFICATION TO SUPERCROSS CATHETER receive FDA 510(k) clearance?

MODIFICATION TO SUPERCROSS CATHETER received FDA 510(k) clearance on 2002-01-11, under 510(k) number K014118.

Who is the listed applicant for MODIFICATION TO SUPERCROSS CATHETER?

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

What is the FDA product code for MODIFICATION TO SUPERCROSS CATHETER?

The FDA product code for MODIFICATION TO SUPERCROSS CATHETER is DQY.

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Other records listing Abbott Vascular, 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.

K123067PROGRESS GUIDE WIRE FAMILY, PILOT GUIDE WIRE FAMILYK122573HI-TORQUE COMMAND GUIDE WIRE FAMILYK102705ARMADA 14 PTA CATHETERK101648HI-TORQUE WINN GUIDE WIRE FAMILYK101011HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSALK091825HI-TORQUE PROGRESS GUIDE WIRE FAMILY

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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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