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FDA 510(k)

C.T.M Mobility Scooter

K-Number: K181344 · 2018-12-14

Decision Date2018-12-14
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

C.T.M Mobility Scooter is a medical device manufactured by Chien TI Enterprise Co., Ltd.. It received FDA 510(k) clearance on 2018-12-14 under approval number K181344. 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 C.T.M Mobility Scooter?

C.T.M Mobility Scooter is a medical device that received FDA 510(k) clearance on 2018-12-14. It is manufactured by Chien TI Enterprise Co., Ltd.. The 510(k) number is K181344.

When was C.T.M Mobility Scooter approved by the FDA?

C.T.M Mobility Scooter received FDA 510(k) clearance on 2018-12-14, under approval number K181344.

What company makes C.T.M Mobility Scooter?

C.T.M Mobility Scooter is manufactured by Chien TI Enterprise Co., Ltd..

What is the FDA product code for C.T.M Mobility Scooter?

The FDA product code for C.T.M Mobility Scooter is INI.

Other Devices by Chien TI Enterprise Co., Ltd.

Related Devices (Code: INI)

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.