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FDA 510(k)

JETi 88 Peripheral Thrombectomy System

K-Number: K183403 · 2019-04-17

Decision Date2019-04-17
Product CodeQEZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JETi 88 Peripheral Thrombectomy System is the device name listed in this FDA 510(k) record. The listed applicant is Walk Vascular, LLC. It received FDA 510(k) clearance on 2019-04-17 under 510(k) number K183403. The device is classified under product code QEZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JETi 88 Peripheral Thrombectomy System?

JETi 88 Peripheral Thrombectomy System is a medical device that received FDA 510(k) clearance on 2019-04-17. The listed applicant is Walk Vascular, LLC. The 510(k) number is K183403.

When did JETi 88 Peripheral Thrombectomy System receive FDA 510(k) clearance?

JETi 88 Peripheral Thrombectomy System received FDA 510(k) clearance on 2019-04-17, under 510(k) number K183403.

Who is the listed applicant for JETi 88 Peripheral Thrombectomy System?

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

What is the FDA product code for JETi 88 Peripheral Thrombectomy System?

The FDA product code for JETi 88 Peripheral Thrombectomy System is QEZ.

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.

Other records listing Walk Vascular, LLC 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.

View all 7 devices →

Related Devices (Code: QEZ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.