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FDA 510(k)

NESS SYSTEM

K-Number: K022776 · 2002-09-11

ApplicantNess-Neuromuscular Electrical Stimulation Systems
Decision Date2002-09-11
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NESS 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 2002-09-11 under 510(k) number K022776. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NESS SYSTEM?

NESS SYSTEM is a medical device that received FDA 510(k) clearance on 2002-09-11. The listed applicant is Ness-Neuromuscular Electrical Stimulation Systems. The 510(k) number is K022776.

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

NESS SYSTEM received FDA 510(k) clearance on 2002-09-11, under 510(k) number K022776.

Who is the listed applicant for NESS 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 SYSTEM?

The FDA product code for NESS SYSTEM is IPF.

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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 L300K031900HANDMASTERK024279NESS CHILDREN SYSTEMK012823MODIFICATION TO HANDMASTER

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Related Devices (Code: IPF)

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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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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