Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200— 510(k) K183290

Name: FDA 510(k) clearance K183290
Creator: U.S. Food and Drug Administration
Published: 2019-02-25

Substantially Equivalent

Thrombolex, Inc.

FDA 510(k) clearance K183290 for Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200, Substantially Equivalent on 2019-02-25. Applicant: Thrombolex, Inc.. Device class: 2.

Clearance details

Applicant: Thrombolex, Inc.
Product code: Code QEY
Device class: Class 2
Regulation: 21 CFR 870.5150
Advisory panel: Cardiovascular
Date received: 2018-11-26
Decision date: 2019-02-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Britain, PA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.