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FDA 510(k)

CONTOUR TECHNOLOGY MUSCLE STIMULATOR

K-Number: K111476 · 2012-05-23

ApplicantContour Technology
Decision Date2012-05-23
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CONTOUR TECHNOLOGY MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Contour Technology. It received FDA 510(k) clearance on 2012-05-23 under 510(k) number K111476. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTOUR TECHNOLOGY MUSCLE STIMULATOR?

CONTOUR TECHNOLOGY MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 2012-05-23. The listed applicant is Contour Technology. The 510(k) number is K111476.

When did CONTOUR TECHNOLOGY MUSCLE STIMULATOR receive FDA 510(k) clearance?

CONTOUR TECHNOLOGY MUSCLE STIMULATOR received FDA 510(k) clearance on 2012-05-23, under 510(k) number K111476.

Who is the listed applicant for CONTOUR TECHNOLOGY MUSCLE STIMULATOR?

The FDA 510(k) record lists Contour Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTOUR TECHNOLOGY MUSCLE STIMULATOR?

The FDA product code for CONTOUR TECHNOLOGY MUSCLE STIMULATOR is NGX.

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Related Devices (Code: NGX)

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.

K253790High Intensity Focused Electromagnetic Stimulation Device (FE60)Beijing Winkonlaser Technology LimitedK253926DiacoreShenB Co., Ltd.K253636Zionic Pro Max (EMS)Termosalud S.L.K253408CoolToneZimmer Medizinsysteme GmbHK252154Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)Guangzhou Longest Medical Technology Co., Ltd.K253478Motive™ Muscle Stimulator for Lower Back (OT01-1003)Motive Health, 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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