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FDA 510(k)

INTERX5000

K-Number: K042912 · 2005-05-17

ApplicantNeuro Resource Group, Inc.
Decision Date2005-05-17
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

INTERX5000 is the device name listed in this FDA 510(k) record. The listed applicant is Neuro Resource Group, Inc.. It received FDA 510(k) clearance on 2005-05-17 under 510(k) number K042912. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERX5000?

INTERX5000 is a medical device that received FDA 510(k) clearance on 2005-05-17. The listed applicant is Neuro Resource Group, Inc.. The 510(k) number is K042912.

When did INTERX5000 receive FDA 510(k) clearance?

INTERX5000 received FDA 510(k) clearance on 2005-05-17, under 510(k) number K042912.

Who is the listed applicant for INTERX5000?

The FDA 510(k) record lists Neuro Resource Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERX5000?

The FDA product code for INTERX5000 is GZJ.

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Other records listing Neuro Resource Group, 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.

K130816INTERX STERILE SELF-ADHESIVE DUAL ELECTRODE (ISSDE)K070217INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USEK053626INTERX500 FLEXIBLE ARRAY ELECTRODE

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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