The Luco Hybrid OSA Appliance— 510(k) K160477

Name: FDA 510(k) clearance K160477
Creator: U.S. Food and Drug Administration
Published: 2016-07-29

Substantially Equivalent

Luco Hybrid Osa Appliance, Inc.

FDA 510(k) clearance K160477 for The Luco Hybrid OSA Appliance, Substantially Equivalent on 2016-07-29. Applicant: Luco Hybrid Osa Appliance, Inc.. Device class: Unclassified.

Clearance details

Applicant: Luco Hybrid Osa Appliance, Inc.
Product code: Code OCO
Device class: Unclassified
Advisory panel: Unknown
Date received: 2016-02-19
Decision date: 2016-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kingston, CA

Download summary PDF View on FDA.gov ↗

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