Frontier X Plus— 510(k) K240794

Name: FDA 510(k) clearance K240794
Creator: U.S. Food and Drug Administration
Published: 2024-11-08

Substantially Equivalent

Fourth Frontier Technologies Pvt, Ltd.

FDA 510(k) clearance K240794 for Frontier X Plus, Substantially Equivalent on 2024-11-08. Applicant: Fourth Frontier Technologies Pvt, Ltd.. Device class: 2.

Clearance details

Applicant: Fourth Frontier Technologies Pvt, Ltd.
Product code: Code MLO
Device class: Class 2
Regulation: 21 CFR 870.2800
Advisory panel: Cardiovascular
Date received: 2024-03-22
Decision date: 2024-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bengaluru, IN

Download summary PDF View on FDA.gov ↗

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