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FDA 510(k)

NEURODYN MULTIWAVE, AUSSIE SPORT

K-Number: K131629 · 2013-11-26

ApplicantIbramed Equipamentos Medicos
Decision Date2013-11-26
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NEURODYN MULTIWAVE, AUSSIE SPORT is the device name listed in this FDA 510(k) record. The listed applicant is Ibramed Equipamentos Medicos. It received FDA 510(k) clearance on 2013-11-26 under 510(k) number K131629. 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 NEURODYN MULTIWAVE, AUSSIE SPORT?

NEURODYN MULTIWAVE, AUSSIE SPORT is a medical device that received FDA 510(k) clearance on 2013-11-26. The listed applicant is Ibramed Equipamentos Medicos. The 510(k) number is K131629.

When did NEURODYN MULTIWAVE, AUSSIE SPORT receive FDA 510(k) clearance?

NEURODYN MULTIWAVE, AUSSIE SPORT received FDA 510(k) clearance on 2013-11-26, under 510(k) number K131629.

Who is the listed applicant for NEURODYN MULTIWAVE, AUSSIE SPORT?

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

What is the FDA product code for NEURODYN MULTIWAVE, AUSSIE SPORT?

The FDA product code for NEURODYN MULTIWAVE, AUSSIE SPORT is IPF.

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Related Devices (Code: IPF)

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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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