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FDA 510(k)

NEW-STIM SPINAL ADJUSTMENT INSTRUMENT

K-Number: K944369 · 1995-04-26

ApplicantLawrence E. Newsum, DC
Decision Date1995-04-26
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

NEW-STIM SPINAL ADJUSTMENT INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Lawrence E. Newsum, DC. It received FDA 510(k) clearance on 1995-04-26 under 510(k) number K944369. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW-STIM SPINAL ADJUSTMENT INSTRUMENT?

NEW-STIM SPINAL ADJUSTMENT INSTRUMENT is a medical device that received FDA 510(k) clearance on 1995-04-26. The listed applicant is Lawrence E. Newsum, DC. The 510(k) number is K944369.

When did NEW-STIM SPINAL ADJUSTMENT INSTRUMENT receive FDA 510(k) clearance?

NEW-STIM SPINAL ADJUSTMENT INSTRUMENT received FDA 510(k) clearance on 1995-04-26, under 510(k) number K944369.

Who is the listed applicant for NEW-STIM SPINAL ADJUSTMENT INSTRUMENT?

The FDA 510(k) record lists Lawrence E. Newsum, DC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEW-STIM SPINAL ADJUSTMENT INSTRUMENT?

The FDA product code for NEW-STIM SPINAL ADJUSTMENT INSTRUMENT 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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