JETi 88 Peripheral Thrombectomy System
K-Number: K183403 · 2019-04-17
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.