ARX Viral Transport Media Collection and Transport System
Summary
Arx Sciences, Inc. received 510(k) clearance for ARX Viral Transport Media Collection and Transport System, a JSM device. Cleared on 2024-03-19.
Details
Source
510(k) Clearance
External ID
K231843
Action Date
2024-03-19
Status
Traditional
Category
device
Product Code
JSM
Product Description
ARX Viral Transport Media Collection and Transport System. Product code: JSM.
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. Arx Sciences, Inc. has received 2 total clearances in our database.
Arx Sciences, Inc. 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 Arx Sciences, Inc. have FDA actions?
Arx Sciences, Inc. 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 "K231843" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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