Quingo Flyte Mobility Scooter
K-Number: K171256 · 2017-06-08
ApplicantAgile Distributors, LLC
Decision Date2017-06-08
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Quingo Flyte Mobility Scooter is a medical device manufactured by Agile Distributors, LLC. It received FDA 510(k) clearance on 2017-06-08 under approval number K171256. 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 Quingo Flyte Mobility Scooter?
Quingo Flyte Mobility Scooter is a medical device that received FDA 510(k) clearance on 2017-06-08. It is manufactured by Agile Distributors, LLC. The 510(k) number is K171256.
When was Quingo Flyte Mobility Scooter approved by the FDA?
Quingo Flyte Mobility Scooter received FDA 510(k) clearance on 2017-06-08, under approval number K171256.
What company makes Quingo Flyte Mobility Scooter?
Quingo Flyte Mobility Scooter is manufactured by Agile Distributors, LLC.
What is the FDA product code for Quingo Flyte Mobility Scooter?
The FDA product code for Quingo Flyte Mobility Scooter 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.