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FDA 510(k)

TAP III ANTI-SNORING DEVICE

K-Number: K062951 · 2006-12-12

Decision Date2006-12-12
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TAP III ANTI-SNORING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Airway Management, Inc.. It received FDA 510(k) clearance on 2006-12-12 under 510(k) number K062951. 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 TAP III ANTI-SNORING DEVICE?

TAP III ANTI-SNORING DEVICE is a medical device that received FDA 510(k) clearance on 2006-12-12. The listed applicant is Airway Management, Inc.. The 510(k) number is K062951.

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

TAP III ANTI-SNORING DEVICE received FDA 510(k) clearance on 2006-12-12, under 510(k) number K062951.

Who is the listed applicant for TAP III ANTI-SNORING DEVICE?

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

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

The FDA product code for TAP III ANTI-SNORING DEVICE is LRK.

Related Clinical Trials

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.

Other records listing Airway Management, 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.

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.

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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