INVENT SNORING DEVICE— 510(k) K120665

Substantially Equivalent

Ventus Medical, Inc.

FDA 510(k) clearance K120665 for INVENT SNORING DEVICE, Substantially Equivalent on 2012-06-12. Applicant: Ventus Medical, Inc.. Device class: 1.

Clearance details

Applicant: Ventus Medical, Inc.
Product code: Code LWF
Device class: Class 1
Regulation: 21 CFR 874.3900
Advisory panel: Ear, Nose, Throat
Date received: 2012-03-05
Decision date: 2012-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hillsborough, CA, US

Download summary PDF View on FDA.gov ↗

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