FL-10000U Respiratory Humidifier
Summary
Flexicare Medical Limited. received 510(k) clearance for FL-10000U Respiratory Humidifier, a BTT device. Cleared on 2026-01-16.
Details
Source
510(k) Clearance
External ID
K251448
Action Date
2026-01-16
Status
Traditional
Category
device
Product Code
BTT
Product Description
FL-10000U Respiratory Humidifier. Product code: BTT.
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 403 device clearances issued this month. Flexicare Medical Limited. has received 2 total clearances in our database.
Flexicare Medical 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 Flexicare Medical Limited. have FDA actions?
Flexicare Medical 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 "K251448" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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