Indego(R)— 510(k) K173530

Substantially Equivalent

Parker-Hannifin Corporation

FDA 510(k) clearance K173530 for Indego(R), Substantially Equivalent on 2018-01-31. 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: 2017-11-15
Decision date: 2018-01-31
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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K152416 — Indego2016-02-26

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