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FDA 510(k)

KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5

K-Number: K922695 · 1992-09-30

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

Device Summary

KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5 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 K922695. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5?

KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5 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 K922695.

When did KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5 receive FDA 510(k) clearance?

KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5 received FDA 510(k) clearance on 1992-09-30, under 510(k) number K922695.

Who is the listed applicant for KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5?

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 PRECISION ADJUSTOR MOD. SHLCP-5?

The FDA product code for KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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-4K922692KINETIC TECHNOLOGY POCKET PRECISION ADJUSTORK922693KINETIC 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

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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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