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FDA 510(k)

INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE

K-Number: K070217 · 2008-04-04

ApplicantNeuro Resource Group, Inc.
Decision Date2008-04-04
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE 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 2008-04-04 under 510(k) number K070217. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE?

INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE is a medical device that received FDA 510(k) clearance on 2008-04-04. The listed applicant is Neuro Resource Group, Inc.. The 510(k) number is K070217.

When did INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE receive FDA 510(k) clearance?

INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE received FDA 510(k) clearance on 2008-04-04, under 510(k) number K070217.

Who is the listed applicant for INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE?

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 INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE?

The FDA product code for INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE is NFO.

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.

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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)K053626INTERX500 FLEXIBLE ARRAY ELECTRODEK042912INTERX5000

Related Devices (Code: NFO)

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.

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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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