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FDA 510(k)

INTERFERENTIAL STIMULATOR, MODEL NETWAVE

K-Number: K031884 · 2003-06-30

ApplicantRyan Telemedicine
Decision Date2003-06-30
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INTERFERENTIAL STIMULATOR, MODEL NETWAVE is the device name listed in this FDA 510(k) record. The listed applicant is Ryan Telemedicine. It received FDA 510(k) clearance on 2003-06-30 under 510(k) number K031884. 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 INTERFERENTIAL STIMULATOR, MODEL NETWAVE?

INTERFERENTIAL STIMULATOR, MODEL NETWAVE is a medical device that received FDA 510(k) clearance on 2003-06-30. The listed applicant is Ryan Telemedicine. The 510(k) number is K031884.

When did INTERFERENTIAL STIMULATOR, MODEL NETWAVE receive FDA 510(k) clearance?

INTERFERENTIAL STIMULATOR, MODEL NETWAVE received FDA 510(k) clearance on 2003-06-30, under 510(k) number K031884.

Who is the listed applicant for INTERFERENTIAL STIMULATOR, MODEL NETWAVE?

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

What is the FDA product code for INTERFERENTIAL STIMULATOR, MODEL NETWAVE?

The FDA product code for INTERFERENTIAL STIMULATOR, MODEL NETWAVE is IPF.

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 Ryan Telemedicine 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.

K030254INTERFERENTIAL STIMULATOR, MODEL RTM1000

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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