UASure II Blood Uric Acid Monitoring System
Summary
Apex BioTechnology Corp. received 510(k) clearance for UASure II Blood Uric Acid Monitoring System, a PTC device. Cleared on 2025-04-04.
Details
Source
510(k) Clearance
External ID
K242209
Action Date
2025-04-04
Status
Traditional
Category
device
Product Code
PTC
Product Description
UASure II Blood Uric Acid Monitoring System. Product code: PTC.
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. Apex BioTechnology Corp. has received 8 total clearances in our database.
Apex BioTechnology Corp. has 8 FDA actions in our database, including 8 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 Apex BioTechnology Corp. have FDA actions?
Apex BioTechnology Corp. has 8 FDA actions in our database, including 0 recalls and 8 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K242209" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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