Aimanfun Lumea Comfort, A-2789/A-3588
Summary
Kam Yuen Plastic Products , Ltd. received 510(k) clearance for Aimanfun Lumea Comfort, A-2789/A-3588, a ONF device. Cleared on 2021-12-02.
Details
Source
510(k) Clearance
External ID
K212907
Action Date
2021-12-02
Status
Special
Category
device
Product Code
ONF
Product Description
Aimanfun Lumea Comfort, A-2789/A-3588. Product code: ONF.
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Kam Yuen Plastic Products , Ltd. has received 4 total clearances in our database.
Kam Yuen Plastic Products , Ltd. has 4 FDA actions in our database, including 4 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Kam Yuen Plastic Products , Ltd. have FDA actions?
Kam Yuen Plastic Products , Ltd. has 4 FDA actions in our database, including 0 recalls and 4 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K212907" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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