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FDA 510(k)

ARTHROSTIM MANIPULATOR

K-Number: K930431 · 1994-07-15

ApplicantFreeman Procedure Seminars
Decision Date1994-07-15
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

ARTHROSTIM MANIPULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Freeman Procedure Seminars. It received FDA 510(k) clearance on 1994-07-15 under 510(k) number K930431. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSTIM MANIPULATOR?

ARTHROSTIM MANIPULATOR is a medical device that received FDA 510(k) clearance on 1994-07-15. The listed applicant is Freeman Procedure Seminars. The 510(k) number is K930431.

When did ARTHROSTIM MANIPULATOR receive FDA 510(k) clearance?

ARTHROSTIM MANIPULATOR received FDA 510(k) clearance on 1994-07-15, under 510(k) number K930431.

Who is the listed applicant for ARTHROSTIM MANIPULATOR?

The FDA 510(k) record lists Freeman Procedure Seminars as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHROSTIM MANIPULATOR?

The FDA product code for ARTHROSTIM MANIPULATOR is LXM.

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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

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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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