Optiflow Oxygen Kit (AA484J)
Summary
Fisher and Paykel Healthcare Limited received 510(k) clearance for Optiflow Oxygen Kit (AA484J), a BTT device. Cleared on 2026-08-27.
Details
Source
510(k) Clearance
External ID
K262268
Action Date
2026-08-27
Status
Special
Category
device
Product Code
BTT
Product Description
Optiflow Oxygen Kit (AA484J). Product code: BTT.
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 445 device clearances issued this month. Fisher and Paykel Healthcare Limited has received 2 total clearances in our database.
Fisher and Paykel Healthcare Limited has 2 FDA actions in our database, including 2 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 Fisher and Paykel Healthcare Limited have FDA actions?
Fisher and Paykel Healthcare Limited has 2 FDA actions in our database, including 0 recalls and 2 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K262268" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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