FDA 510(k)

THE ODFS DROPPED FOOT STIMULATOR

K-Number: K050991 · 2005-07-15

ApplicantDepartment of Medical Physics and Biomedical Eng.

Decision Date2005-07-15

Product CodeGZI

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

THE ODFS DROPPED FOOT STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Department of Medical Physics and Biomedical Eng.. It received FDA 510(k) clearance on 2005-07-15 under 510(k) number K050991. The device is classified under product code GZI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE ODFS DROPPED FOOT STIMULATOR?

THE ODFS DROPPED FOOT STIMULATOR is a medical device that received FDA 510(k) clearance on 2005-07-15. The listed applicant is Department of Medical Physics and Biomedical Eng.. The 510(k) number is K050991.

When did THE ODFS DROPPED FOOT STIMULATOR receive FDA 510(k) clearance?

THE ODFS DROPPED FOOT STIMULATOR received FDA 510(k) clearance on 2005-07-15, under 510(k) number K050991.

Who is the listed applicant for THE ODFS DROPPED FOOT STIMULATOR?

The FDA 510(k) record lists Department of Medical Physics and Biomedical Eng. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE ODFS DROPPED FOOT STIMULATOR?

The FDA product code for THE ODFS DROPPED FOOT STIMULATOR is GZI.

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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.