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FDA 510(k)

IMPULSE IQ ADJUSTING INSTRUMENT

K-Number: K080261 · 2008-04-11

ApplicantNeuromechanical Innovations, LLC
Decision Date2008-04-11
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

IMPULSE IQ ADJUSTING INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Neuromechanical Innovations, LLC. It received FDA 510(k) clearance on 2008-04-11 under 510(k) number K080261. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPULSE IQ ADJUSTING INSTRUMENT?

IMPULSE IQ ADJUSTING INSTRUMENT is a medical device that received FDA 510(k) clearance on 2008-04-11. The listed applicant is Neuromechanical Innovations, LLC. The 510(k) number is K080261.

When did IMPULSE IQ ADJUSTING INSTRUMENT receive FDA 510(k) clearance?

IMPULSE IQ ADJUSTING INSTRUMENT received FDA 510(k) clearance on 2008-04-11, under 510(k) number K080261.

Who is the listed applicant for IMPULSE IQ ADJUSTING INSTRUMENT?

The FDA 510(k) record lists Neuromechanical Innovations, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPULSE IQ ADJUSTING INSTRUMENT?

The FDA product code for IMPULSE IQ ADJUSTING INSTRUMENT is LXM.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Neuromechanical Innovations, LLC 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.

K023462IMPULSE-ADJUSTING INSTRUMENT, CBP ADJUSTING INSTRUMENT, NEUROMECHANICAL ADJUSTING INSTRUMENT, MODELS 2003

Related Devices (Code: LXM)

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.

K234036SONIK MONARK 100Neuro Spinal Innovation, Inc.K192629SpinalyticsOptima Health Solutions International Corp.K172536Atlas Percussion Adjusting InstrumentSpinalight, Inc.K160278VSTAAR AdjusteRSpinal Acoustics, LLCK112606ACTIVATOR V-EActivator Methods International, Ltd.K082218MAX ADJUSTING INSTRUMENTManna Omni International, Inc.

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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