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FDA 510(k)

SNORE-NO-MORE

K-Number: K922818 · 1994-02-09

ApplicantGreat Lakes Orthodontics, Ltd.
Decision Date1994-02-09
Product CodeLQZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SNORE-NO-MORE is the device name listed in this FDA 510(k) record. The listed applicant is Great Lakes Orthodontics, Ltd.. It received FDA 510(k) clearance on 1994-02-09 under 510(k) number K922818. 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 SNORE-NO-MORE?

SNORE-NO-MORE is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Great Lakes Orthodontics, Ltd.. The 510(k) number is K922818.

When did SNORE-NO-MORE receive FDA 510(k) clearance?

SNORE-NO-MORE received FDA 510(k) clearance on 1994-02-09, under 510(k) number K922818.

Who is the listed applicant for SNORE-NO-MORE?

The FDA 510(k) record lists Great Lakes Orthodontics, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SNORE-NO-MORE?

The FDA product code for SNORE-NO-MORE is LQZ.

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Other records listing Great Lakes Orthodontics, Ltd. as applicant

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Related Devices (Code: LQZ)

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Official Source

View on FDA Database →

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

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