FDA 510(k)

MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WHEEL SCOOTER, MODEL SC940V

K-Number: K091113 · 2009-05-11

Decision Date2009-05-11

Product CodeINI

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WHEEL SCOOTER, MODEL SC940V is the device name listed in this FDA 510(k) record. The listed applicant is Pride Mobility Products Corp.. It received FDA 510(k) clearance on 2009-05-11 under 510(k) number K091113. 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 MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WHEEL SCOOTER, MODEL SC940V?

MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WHEEL SCOOTER, MODEL SC940V is a medical device that received FDA 510(k) clearance on 2009-05-11. The listed applicant is Pride Mobility Products Corp.. The 510(k) number is K091113.

When did MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WHEEL SCOOTER, MODEL SC940V receive FDA 510(k) clearance?

MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WHEEL SCOOTER, MODEL SC940V received FDA 510(k) clearance on 2009-05-11, under 510(k) number K091113.

Who is the listed applicant for MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WHEEL SCOOTER, MODEL SC940V?

The FDA 510(k) record lists Pride Mobility Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WHEEL SCOOTER, MODEL SC940V?

The FDA product code for MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WHEEL SCOOTER, MODEL SC940V is INI.

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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.