Companion— 510(k) DEN140033

Unknown

Lgch, Inc.

FDA 510(k) clearance DEN140033 for Companion, Unknown on 2017-02-16. Applicant: Lgch, Inc.. Device class: 2.

Clearance details

Applicant: Lgch, Inc.
Product code: Code POS
Device class: Class 2
Regulation: 21 CFR 882.1580
Advisory panel: Neurology
Date received: 2014-11-10
Decision date: 2017-02-16
Decision: Unknown
Clearance type: Direct
Location: San Antonio, TX, US

View on FDA.gov ↗

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