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FDA 510(k)

KHAN KINETIC TREATMENT DEVICE (KKT-M1)

K-Number: K060043 · 2006-03-23

ApplicantOptima Health Solutions International, Inc.
Decision Date2006-03-23
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

KHAN KINETIC TREATMENT DEVICE (KKT-M1) is the device name listed in this FDA 510(k) record. The listed applicant is Optima Health Solutions International, Inc.. It received FDA 510(k) clearance on 2006-03-23 under 510(k) number K060043. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KHAN KINETIC TREATMENT DEVICE (KKT-M1)?

KHAN KINETIC TREATMENT DEVICE (KKT-M1) is a medical device that received FDA 510(k) clearance on 2006-03-23. The listed applicant is Optima Health Solutions International, Inc.. The 510(k) number is K060043.

When did KHAN KINETIC TREATMENT DEVICE (KKT-M1) receive FDA 510(k) clearance?

KHAN KINETIC TREATMENT DEVICE (KKT-M1) received FDA 510(k) clearance on 2006-03-23, under 510(k) number K060043.

Who is the listed applicant for KHAN KINETIC TREATMENT DEVICE (KKT-M1)?

The FDA 510(k) record lists Optima Health Solutions International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KHAN KINETIC TREATMENT DEVICE (KKT-M1)?

The FDA product code for KHAN KINETIC TREATMENT DEVICE (KKT-M1) 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.

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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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