Indego— 510(k) K152416

Substantially Equivalent

Parker Hannifin Corporation

FDA 510(k) clearance K152416 for Indego, Substantially Equivalent on 2016-02-26. Applicant: Parker Hannifin Corporation. Device class: 2.

Clearance details

Applicant: Parker Hannifin Corporation
Product code: Code PHL
Device class: Class 2
Regulation: 21 CFR 890.3480
Advisory panel: Physical Medicine
Date received: 2015-08-26
Decision date: 2016-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Macedonia, OH, US

Download summary PDF View on FDA.gov ↗

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More clearances from Parker Hannifin Corporation

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K171334 — Indego2017-09-08

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