Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

GO GO ELITE TRAVELER V THREE WHEEL SCOOTER, MODEL SC40EV

K-Number: K090524 · 2009-03-19

Decision Date2009-03-19
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GO GO ELITE TRAVELER V THREE WHEEL SCOOTER, MODEL SC40EV 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 2009-03-19 under 510(k) number K090524. 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 GO GO ELITE TRAVELER V THREE WHEEL SCOOTER, MODEL SC40EV?

GO GO ELITE TRAVELER V THREE WHEEL SCOOTER, MODEL SC40EV is a medical device that received FDA 510(k) clearance on 2009-03-19. The listed applicant is Pride Mobility Products Corp.. The 510(k) number is K090524.

When did GO GO ELITE TRAVELER V THREE WHEEL SCOOTER, MODEL SC40EV receive FDA 510(k) clearance?

GO GO ELITE TRAVELER V THREE WHEEL SCOOTER, MODEL SC40EV received FDA 510(k) clearance on 2009-03-19, under 510(k) number K090524.

Who is the listed applicant for GO GO ELITE TRAVELER V THREE WHEEL SCOOTER, MODEL SC40EV?

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 GO GO ELITE TRAVELER V THREE WHEEL SCOOTER, MODEL SC40EV?

The FDA product code for GO GO ELITE TRAVELER V THREE WHEEL SCOOTER, MODEL SC40EV is INI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Pride Mobility Products Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 20 devices →

Related Devices (Code: INI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

↑