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FDA 510(k)

NESS CHILDREN SYSTEM

K-Number: K024279 · 2003-02-05

ApplicantNess-Neuromuscular Electrical Stimulation Systems
Decision Date2003-02-05
Product CodeIPG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NESS CHILDREN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ness-Neuromuscular Electrical Stimulation Systems. It received FDA 510(k) clearance on 2003-02-05 under 510(k) number K024279. The device is classified under product code IPG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NESS CHILDREN SYSTEM?

NESS CHILDREN SYSTEM is a medical device that received FDA 510(k) clearance on 2003-02-05. The listed applicant is Ness-Neuromuscular Electrical Stimulation Systems. The 510(k) number is K024279.

When did NESS CHILDREN SYSTEM receive FDA 510(k) clearance?

NESS CHILDREN SYSTEM received FDA 510(k) clearance on 2003-02-05, under 510(k) number K024279.

Who is the listed applicant for NESS CHILDREN SYSTEM?

The FDA 510(k) record lists Ness-Neuromuscular Electrical Stimulation Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NESS CHILDREN SYSTEM?

The FDA product code for NESS CHILDREN SYSTEM is IPG.

Related Clinical Trials

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Other records listing Ness-Neuromuscular Electrical Stimulation Systems 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.

K111767NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KITK080219MODIFICATION TO:NESS L300K053468NESS L300K031900HANDMASTERK022776NESS SYSTEMK012823MODIFICATION TO HANDMASTER

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Related Devices (Code: IPG)

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.

K790652TOGUARDTogard, Inc.K781363CAST SHOECutler BiomedicalK780617EQUALIZERBallert Orthopedic Corp.K760575ROCKER-SOLE CAST SANDALRichard'S Medical Equip., Inc.K760578BALANCED CAST SOLEParke-Davis Co.

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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