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FDA 510(k)

KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR

K-Number: K922692 · 1992-09-30

ApplicantKinetic Technology, Inc.
Decision Date1992-09-30
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Technology, Inc.. It received FDA 510(k) clearance on 1992-09-30 under 510(k) number K922692. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR?

KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR is a medical device that received FDA 510(k) clearance on 1992-09-30. The listed applicant is Kinetic Technology, Inc.. The 510(k) number is K922692.

When did KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR receive FDA 510(k) clearance?

KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR received FDA 510(k) clearance on 1992-09-30, under 510(k) number K922692.

Who is the listed applicant for KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR?

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

What is the FDA product code for KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR?

The FDA product code for KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR 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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Other records listing Kinetic Technology, Inc. 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.

K922694KINETIC TECHNOLOGY PRECISION ADUSTOR MODEL SHLCP-4K922695KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5K922693KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1K870910PRECISION SPINAL ADJUSTER MODEL 115

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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