Atrieve™ Vascular Snare Kit

Atrieve™ Vascular Snare Kit 3.2F

Registry build 21.09.26
1manufacturer
7catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

Registered in Guangdong.

Chinese manufacturers registered for FDA product code MMX
Manufacturer City Province Registered as Device types
Lifetech Scientific (Shenzhen) Co,.ltd Shenzhen Guangdong Manufacturer 3

Record

Regulatory record for Atrieve™ Vascular Snare Kit
Listed by Argon Medical Devices, Inc., United States
FDA product code MMX
Device type Device, Percutaneous Retrieval
Device class Class 2
Regulation 21 CFR 870.5150
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer
510(k) K021606
Record published 2016-09-20
Record revised 2026-05-11 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Keep Dry and Away from Sunlight

Catalogue Numbers

Catalogue numbers for Atrieve™ Vascular Snare Kit
Catalogue number Size Status
382006010 6F In distribution
382006020 6F In distribution
381003004 3.2F In distribution
381003008 3.2F In distribution
382006015 6F In distribution
382007030 7F In distribution
382007045 7F In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ONE Snare® Merit Medical Systems, Inc. 29
EN Snare® Merit Medical Systems, Inc. 17
SeQureTM Snare System Lifetech Scientific (Shenzhen) Co,.ltd 12
Expro Elite Teleflex Medical LLC 10
Halo™ Single Loop Snare Kit Argon Medical Devices, Inc. 9
Halo™ Single-Loop Microsnare Kit Argon Medical Devices, Inc. 6
Expro Elite™ snare Vascular Solutions LLC 5
Amplatz Goose Neck™ Medtronic, Inc. 5
Sympro Elite Teleflex Medical LLC 5
Quattro Elite™ snare Vascular Solutions LLC 5
Sympro Elite™ snare Vascular Solutions LLC 5
Empower™ Merit Medical Systems, Inc. 4

Showing 12 of 26. All products under Device, Percutaneous Retrieval

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K232443 2023-09-07
K200963 2021-01-05
K200268 2020-06-03
K191758 2019-12-17

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer