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FDA 510(k)

MAX ADJUSTING INSTRUMENT

K-Number: K082218 · 2008-08-13

ApplicantManna Omni International, Inc.
Decision Date2008-08-13
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

MAX ADJUSTING INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Manna Omni International, Inc.. It received FDA 510(k) clearance on 2008-08-13 under 510(k) number K082218. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAX ADJUSTING INSTRUMENT?

MAX ADJUSTING INSTRUMENT is a medical device that received FDA 510(k) clearance on 2008-08-13. The listed applicant is Manna Omni International, Inc.. The 510(k) number is K082218.

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

MAX ADJUSTING INSTRUMENT received FDA 510(k) clearance on 2008-08-13, under 510(k) number K082218.

Who is the listed applicant for MAX ADJUSTING INSTRUMENT?

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

What is the FDA product code for MAX ADJUSTING INSTRUMENT?

The FDA product code for MAX ADJUSTING INSTRUMENT is LXM.

Related Clinical Trials

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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.K080261IMPULSE IQ ADJUSTING INSTRUMENTNeuromechanical Innovations, LLC

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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