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FDA 510(k)

Electric wheelchair (S7018)

K-Number: K240270 · 2024-08-27

ApplicantGuangdong Prestige Technology Company Limited
Decision Date2024-08-27
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electric wheelchair (S7018) is a medical device manufactured by Guangdong Prestige Technology Company Limited. It received FDA 510(k) clearance on 2024-08-27 under approval number K240270. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Electric wheelchair (S7018)?

Electric wheelchair (S7018) is a medical device that received FDA 510(k) clearance on 2024-08-27. It is manufactured by Guangdong Prestige Technology Company Limited. The 510(k) number is K240270.

When was Electric wheelchair (S7018) approved by the FDA?

Electric wheelchair (S7018) received FDA 510(k) clearance on 2024-08-27, under approval number K240270.

What company makes Electric wheelchair (S7018)?

Electric wheelchair (S7018) is manufactured by Guangdong Prestige Technology Company Limited.

What is the FDA product code for Electric wheelchair (S7018)?

The FDA product code for Electric wheelchair (S7018) is ITI.

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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.

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