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FDA 510(k)

Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP Catheter

K-Number: K261825 · 2026-07-02

ApplicantAbbott
Decision Date2026-07-02
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Abbott. It received FDA 510(k) clearance on 2026-07-02 under 510(k) number K261825. 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 Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP Catheter?

Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP Catheter is a medical device that received FDA 510(k) clearance on 2026-07-02. The listed applicant is Abbott. The 510(k) number is K261825.

When did Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP Catheter receive FDA 510(k) clearance?

Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP Catheter received FDA 510(k) clearance on 2026-07-02, under 510(k) number K261825.

Who is the listed applicant for Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP Catheter?

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

What is the FDA product code for Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP Catheter?

The FDA product code for Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP Catheter is DQY.

Other records listing Abbott 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.

PMA P170038Ventricular (assist) bypassK260993Amplatzer TorqVue Delivery SystemK251221Assert-IQ (DM5000); Assert-IQ (DM5300); Assert-IQ (DM5500); Merlin.net (MN7000)K233655Lingo Glucose SystemK222297CentriMag Pre-connected PackK221213EnSite X EP System

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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.

K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261631Amplatzer TorqVue Exchange SystemAbbott MedicalK260289Perfect-O Ostial Positioning CatheterBalosmark, Inc.

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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