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FDA 510(k)

NTI TENSION SUPPRESSION SYSTEM

K-Number: K010876 · 2001-06-20

ApplicantNti-Tss, Inc.
Decision Date2001-06-20
Product CodeOCO
DecisionSubstantially Equivalent

Device Summary

NTI TENSION SUPPRESSION SYSTEM 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 2001-06-20 under 510(k) number K010876. The device is classified under product code OCO. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NTI TENSION SUPPRESSION SYSTEM?

NTI TENSION SUPPRESSION SYSTEM is a medical device that received FDA 510(k) clearance on 2001-06-20. The listed applicant is Nti-Tss, Inc.. The 510(k) number is K010876.

When did NTI TENSION SUPPRESSION SYSTEM receive FDA 510(k) clearance?

NTI TENSION SUPPRESSION SYSTEM received FDA 510(k) clearance on 2001-06-20, under 510(k) number K010876.

Who is the listed applicant for NTI TENSION SUPPRESSION SYSTEM?

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?

The FDA product code for NTI TENSION SUPPRESSION SYSTEM is OCO.

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.

K041184NTI TENSION SUPPRESSION SYSTEM, WITH A SNOREHOOK APPLICATION

Related Devices (Code: OCO)

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.

K202523TMJ RelaxMoonwalker Innovations, Inc.K160477The Luco Hybrid OSA ApplianceLuco Hybrid Osa Appliance, Inc.

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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