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FDA 510(k)

NTI TENSION SUPPRESSION SYSTEM, WITH A SNOREHOOK APPLICATION

K-Number: K041184 · 2005-05-03

ApplicantNti-Tss, Inc.
Decision Date2005-05-03
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NTI TENSION SUPPRESSION SYSTEM, WITH A SNOREHOOK APPLICATION is the device name listed in this FDA 510(k) record. The listed applicant is Nti-Tss, Inc.. It received FDA 510(k) clearance on 2005-05-03 under 510(k) number K041184. 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 NTI TENSION SUPPRESSION SYSTEM, WITH A SNOREHOOK APPLICATION?

NTI TENSION SUPPRESSION SYSTEM, WITH A SNOREHOOK APPLICATION is a medical device that received FDA 510(k) clearance on 2005-05-03. The listed applicant is Nti-Tss, Inc.. The 510(k) number is K041184.

When did NTI TENSION SUPPRESSION SYSTEM, WITH A SNOREHOOK APPLICATION receive FDA 510(k) clearance?

NTI TENSION SUPPRESSION SYSTEM, WITH A SNOREHOOK APPLICATION received FDA 510(k) clearance on 2005-05-03, under 510(k) number K041184.

Who is the listed applicant for NTI TENSION SUPPRESSION SYSTEM, WITH A SNOREHOOK APPLICATION?

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

What is the FDA product code for NTI TENSION SUPPRESSION SYSTEM, WITH A SNOREHOOK APPLICATION?

The FDA product code for NTI TENSION SUPPRESSION SYSTEM, WITH A SNOREHOOK APPLICATION 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.

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Other records listing Nti-Tss, 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.

K010876NTI TENSION SUPPRESSION SYSTEM

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

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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