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FDA 510(k)

MUSMATE WALKING AID

K-Number: K073521 · 2008-02-04

ApplicantMusmate, Ltd.
Decision Date2008-02-04
Product CodeOHI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MUSMATE WALKING AID is the device name listed in this FDA 510(k) record. The listed applicant is Musmate, Ltd.. It received FDA 510(k) clearance on 2008-02-04 under 510(k) number K073521. The device is classified under product code OHI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUSMATE WALKING AID?

MUSMATE WALKING AID is a medical device that received FDA 510(k) clearance on 2008-02-04. The listed applicant is Musmate, Ltd.. The 510(k) number is K073521.

When did MUSMATE WALKING AID receive FDA 510(k) clearance?

MUSMATE WALKING AID received FDA 510(k) clearance on 2008-02-04, under 510(k) number K073521.

Who is the listed applicant for MUSMATE WALKING AID?

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

What is the FDA product code for MUSMATE WALKING AID?

The FDA product code for MUSMATE WALKING AID is OHI.

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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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