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FDA 510(k)

MILLENIUM ANTI-SNORING DEVICE

K-Number: K112627 · 2012-06-06

ApplicantMillenium Dental Laboratory, Inc.
Decision Date2012-06-06
Product CodeLQZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MILLENIUM ANTI-SNORING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Millenium Dental Laboratory, Inc.. It received FDA 510(k) clearance on 2012-06-06 under 510(k) number K112627. The device is classified under product code LQZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLENIUM ANTI-SNORING DEVICE?

MILLENIUM ANTI-SNORING DEVICE is a medical device that received FDA 510(k) clearance on 2012-06-06. The listed applicant is Millenium Dental Laboratory, Inc.. The 510(k) number is K112627.

When did MILLENIUM ANTI-SNORING DEVICE receive FDA 510(k) clearance?

MILLENIUM ANTI-SNORING DEVICE received FDA 510(k) clearance on 2012-06-06, under 510(k) number K112627.

Who is the listed applicant for MILLENIUM ANTI-SNORING DEVICE?

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

What is the FDA product code for MILLENIUM ANTI-SNORING DEVICE?

The FDA product code for MILLENIUM ANTI-SNORING DEVICE is LQZ.

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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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