Jintronix— 510(k) K143034

Substantially Equivalent

Jintronix, Inc.

FDA 510(k) clearance K143034 for Jintronix, Substantially Equivalent on 2015-04-22. Applicant: Jintronix, Inc.. Device class: 2.

Clearance details

Applicant: Jintronix, Inc.
Product code: Code LXJ
Device class: Class 2
Regulation: 21 CFR 890.5360
Advisory panel: Physical Medicine
Date received: 2014-10-22
Decision date: 2015-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Jintronix, Inc.

K130847 — JINTRONIX REHABILITATION SYSTEM (JRS)2014-02-28

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