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FDA 510(k)

THE SNORE PEACE

K-Number: K981923 · 1998-08-24

ApplicantThe Snore Peace Group
Decision Date1998-08-24
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE SNORE PEACE is the device name listed in this FDA 510(k) record. The listed applicant is The Snore Peace Group. It received FDA 510(k) clearance on 1998-08-24 under 510(k) number K981923. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SNORE PEACE?

THE SNORE PEACE is a medical device that received FDA 510(k) clearance on 1998-08-24. The listed applicant is The Snore Peace Group. The 510(k) number is K981923.

When did THE SNORE PEACE receive FDA 510(k) clearance?

THE SNORE PEACE received FDA 510(k) clearance on 1998-08-24, under 510(k) number K981923.

Who is the listed applicant for THE SNORE PEACE?

The FDA 510(k) record lists The Snore Peace Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE SNORE PEACE?

The FDA product code for THE SNORE PEACE is LRK.

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Related Devices (Code: LRK)

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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