Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1

K-Number: K922693 · 1992-09-30

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

Device Summary

KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1 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 K922693. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1?

KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1 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 K922693.

When did KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1 receive FDA 510(k) clearance?

KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1 received FDA 510(k) clearance on 1992-09-30, under 510(k) number K922693.

Who is the listed applicant for KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1?

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 TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1?

The FDA product code for KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1 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-4K922695KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5K922692KINETIC TECHNOLOGY POCKET PRECISION ADJUSTORK870910PRECISION 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.

↑