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FDA 510(k)

WAVELENGHT ULTRASOUND LOTION

K-Number: K013212 · 2002-02-25

ApplicantNational Therapy Products, Inc.
Decision Date2002-02-25
Product CodeMUI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WAVELENGHT ULTRASOUND LOTION is the device name listed in this FDA 510(k) record. The listed applicant is National Therapy Products, Inc.. It received FDA 510(k) clearance on 2002-02-25 under 510(k) number K013212. The device is classified under product code MUI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WAVELENGHT ULTRASOUND LOTION?

WAVELENGHT ULTRASOUND LOTION is a medical device that received FDA 510(k) clearance on 2002-02-25. The listed applicant is National Therapy Products, Inc.. The 510(k) number is K013212.

When did WAVELENGHT ULTRASOUND LOTION receive FDA 510(k) clearance?

WAVELENGHT ULTRASOUND LOTION received FDA 510(k) clearance on 2002-02-25, under 510(k) number K013212.

Who is the listed applicant for WAVELENGHT ULTRASOUND LOTION?

The FDA 510(k) record lists National Therapy Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WAVELENGHT ULTRASOUND LOTION?

The FDA product code for WAVELENGHT ULTRASOUND LOTION is MUI.

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 National Therapy Products, 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.

K012522WAVELENGTH MULTI-PURPOSE ULTRASOUND GEL

Related Devices (Code: MUI)

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.

K253255Non-Sterile Ultrasound Gel Sterile Ultrasound GelFoshan Pingchuang Medical Technology Co., Ltd.K252337EdgeFlow Gel PadEdgecare, Inc.K242167Sterile and Non-Sterile Ultrasonic Coupling AgentAnhui Deepblue Medical Technology Co., Ltd.K241789Non-Sterile Ultrasound Transmission GelsHony Medical Co., Ltd.K232957Sterile and Non-Sterile Ultrasound GelsJianerkang Medical Co., Ltd.K221999Ultrasound Transmission GelsHony Medical Co., Ltd.

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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