Airdog X5 Recirculating Air Cleaner (model KJ300F-X5)
Summary
Beiang Air Tech , Ltd. received 510(k) clearance for Airdog X5 Recirculating Air Cleaner (model KJ300F-X5), a FRF device. Cleared on 2022-11-22.
Details
Source
510(k) Clearance
External ID
K211507
Action Date
2022-11-22
Status
Traditional
Category
device
Product Code
FRF
Product Description
Airdog X5 Recirculating Air Cleaner (model KJ300F-X5). Product code: FRF.
Company
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 534 device clearances issued this month.
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 Beiang Air Tech , Ltd. have FDA actions?
This is the only FDA action we have on record for Beiang Air Tech , Ltd. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K211507" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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