FDA.reportPublic FDA data

510(k) K232443

Device
Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit
Applicant
Argon Medical Devices, Inc.
510(k) number
K232443
Product code
MMX
Decision
Substantially Equivalent (SESE)
Decision date
2023-09-07
Date received
2023-08-14
Regulation
870.5150
Classification name
Device, Percutaneous Retrieval
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Ana Jimenez-Hughes
Address
1445 Flat Creek Rd. Athens TX US 75751 75751

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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