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FDA 510(k)

ACTIVATOR V-E

K-Number: K112606 · 2012-03-06

ApplicantActivator Methods International, Ltd.
Decision Date2012-03-06
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

ACTIVATOR V-E is the device name listed in this FDA 510(k) record. The listed applicant is Activator Methods International, Ltd.. It received FDA 510(k) clearance on 2012-03-06 under 510(k) number K112606. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTIVATOR V-E?

ACTIVATOR V-E is a medical device that received FDA 510(k) clearance on 2012-03-06. The listed applicant is Activator Methods International, Ltd.. The 510(k) number is K112606.

When did ACTIVATOR V-E receive FDA 510(k) clearance?

ACTIVATOR V-E received FDA 510(k) clearance on 2012-03-06, under 510(k) number K112606.

Who is the listed applicant for ACTIVATOR V-E?

The FDA 510(k) record lists Activator Methods International, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACTIVATOR V-E?

The FDA product code for ACTIVATOR V-E is LXM.

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Other records listing Activator Methods International, Ltd. 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.

K072519ACTIVATOR V SPINAL ADJUSTING INSTRUMENTK003185FS ACTIVATOR III

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, LLCK082218MAX ADJUSTING INSTRUMENTManna Omni International, Inc.K080261IMPULSE IQ ADJUSTING INSTRUMENTNeuromechanical Innovations, LLC

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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