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FDA PMA

Ventricular (assist) bypass

PMA Number: P170038 · 2026-10-02

ApplicantAbbott
Decision Date2026-10-02
PMA NumberP170038
Product CodeDSQ
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeCV

Device Summary

Ventricular (assist) bypass is the device name listed in this FDA 510(k) record. The listed applicant is Abbott. It received FDA 510(k) clearance on 2026-10-02. The device is classified under product code DSQ. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Ventricular (assist) bypass?

Ventricular (assist) bypass is a medical device that received FDA 510(k) clearance on 2026-10-02. The listed applicant is Abbott.

When did Ventricular (assist) bypass receive FDA 510(k) clearance?

The clearance date for Ventricular (assist) bypass can be found in the official FDA records.

Who is the listed applicant for Ventricular (assist) bypass?

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 Ventricular (assist) bypass?

The FDA product code for Ventricular (assist) bypass is DSQ.

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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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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