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FDA 510(k)

INVENT SNORING DEVICE

K-Number: K120665 · 2012-06-12

ApplicantVentus Medical, Inc.
Decision Date2012-06-12
Product CodeLWF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

INVENT SNORING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Ventus Medical, Inc.. It received FDA 510(k) clearance on 2012-06-12 under 510(k) number K120665. The device is classified under product code LWF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INVENT SNORING DEVICE?

INVENT SNORING DEVICE is a medical device that received FDA 510(k) clearance on 2012-06-12. The listed applicant is Ventus Medical, Inc.. The 510(k) number is K120665.

When did INVENT SNORING DEVICE receive FDA 510(k) clearance?

INVENT SNORING DEVICE received FDA 510(k) clearance on 2012-06-12, under 510(k) number K120665.

Who is the listed applicant for INVENT SNORING DEVICE?

The FDA 510(k) record lists Ventus Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INVENT SNORING DEVICE?

The FDA product code for INVENT SNORING DEVICE is LWF.

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Other records listing Ventus Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: LWF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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