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Atrieve™ Vascular Snare Kit

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Atrieve™ Vascular Snare Kit FDA UDI
Generic Name
Intravascular extraction catheter-snare FDA UDI
Device Name
Atrieve™ Vascular Snare Kit 6F FDA UDI
Model / Reference
382006015 FDA UDI
Description
Atrieve™ Vascular Snare Kit 6F FDA UDI

Identifiers

Catalog Number
382006015 FDA UDI
Primary DI / UDI-DI
20886333004021 FDA UDI
510(k) Number
K021606 FDA UDI
FDA Product Code
MMX FDA UDI
GMDN Term
Intravascular extraction catheter-snare FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intravascular extraction catheter-snare

Atrieve™ Vascular Snare Kit by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravascular extraction catheter-snare.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6a6c1a7a-9a75-407e-b061-6906d14c6003 38 fields · synced Jun 9, 2026