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FDA 510(k)

Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588

K-Number: K230107 · 2023-04-05

Decision Date2023-04-05
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588 is a medical device manufactured by Kam Yuen Plastic Products , Ltd.. It received FDA 510(k) clearance on 2023-04-05 under approval number K230107. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588?

Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588 is a medical device that received FDA 510(k) clearance on 2023-04-05. It is manufactured by Kam Yuen Plastic Products , Ltd.. The 510(k) number is K230107.

When was Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588 approved by the FDA?

Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588 received FDA 510(k) clearance on 2023-04-05, under approval number K230107.

What company makes Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588?

Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588 is manufactured by Kam Yuen Plastic Products , Ltd..

What is the FDA product code for Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588?

The FDA product code for Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588 is OHT.

Related Clinical Trials

Other Devices by Kam Yuen Plastic Products , Ltd.

Related Devices (Code: OHT)

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.