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FDA 510(k)

FYMCO FLYER

K-Number: K915416 · 1992-08-03

ApplicantMotion Dynamics
Decision Date1992-08-03
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FYMCO FLYER is the device name listed in this FDA 510(k) record. The listed applicant is Motion Dynamics. It received FDA 510(k) clearance on 1992-08-03 under 510(k) number K915416. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FYMCO FLYER?

FYMCO FLYER is a medical device that received FDA 510(k) clearance on 1992-08-03. The listed applicant is Motion Dynamics. The 510(k) number is K915416.

When did FYMCO FLYER receive FDA 510(k) clearance?

FYMCO FLYER received FDA 510(k) clearance on 1992-08-03, under 510(k) number K915416.

Who is the listed applicant for FYMCO FLYER?

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

What is the FDA product code for FYMCO FLYER?

The FDA product code for FYMCO FLYER is INI.

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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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