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FDA 510(k)

MA-300 ELECTROMYOGRAPHY SYSTEM

K-Number: K000220 · 2000-02-24

ApplicantMotion Lab Systems, Inc.
Decision Date2000-02-24
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MA-300 ELECTROMYOGRAPHY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Motion Lab Systems, Inc.. It received FDA 510(k) clearance on 2000-02-24 under 510(k) number K000220. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MA-300 ELECTROMYOGRAPHY SYSTEM?

MA-300 ELECTROMYOGRAPHY SYSTEM is a medical device that received FDA 510(k) clearance on 2000-02-24. The listed applicant is Motion Lab Systems, Inc.. The 510(k) number is K000220.

When did MA-300 ELECTROMYOGRAPHY SYSTEM receive FDA 510(k) clearance?

MA-300 ELECTROMYOGRAPHY SYSTEM received FDA 510(k) clearance on 2000-02-24, under 510(k) number K000220.

Who is the listed applicant for MA-300 ELECTROMYOGRAPHY SYSTEM?

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

What is the FDA product code for MA-300 ELECTROMYOGRAPHY SYSTEM?

The FDA product code for MA-300 ELECTROMYOGRAPHY SYSTEM is IKN.

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 Motion Lab Systems, 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.

K974385MLS ELECTROMYOGRAPHIC PREAMPLIFIER

Related Devices (Code: IKN)

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.

K172743Natus VikingQuestNatus Neurology IncorporatedK163150ViMove2Dorsavi, Ltd.K162383Cadwell Sierra Summit, Cadwell Sierra AscentCadwell Industries, Inc.K123902PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)Oktx, LLCK123399MYOVISION 3.0 WIREFREE SYSTEMPrecision Biometrics, Inc.K113074CMAP PROMedical Technologies, 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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