Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit
Summary
Argon Medical Devices, Inc. received 510(k) clearance for Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit, a MMX device. Cleared on 2023-09-07.
Details
Source
510(k) Clearance
External ID
K232443
Action Date
2023-09-07
Status
Special
Category
device
Product Code
MMX
Product Description
Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit. Product code: MMX.
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. Argon Medical Devices, Inc. has received 12 total clearances in our database.
Argon Medical Devices, Inc. has 19 FDA actions in our database, including 7 recalls and 12 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 Argon Medical Devices, Inc. have FDA actions?
Argon Medical Devices, Inc. has 19 FDA actions in our database, including 7 recalls and 12 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K232443" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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