Empower™

4 catalogue numbers from 00884450269206, listed by Merit Medical Systems, Inc., United States, under Device, Percutaneous Retrieval. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
4catalogue numbers in this listing
5510(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 Empower™
Listed by Merit Medical Systems, 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, Complaint-file establishment, Manufacturer, Exporter
Record published 2017-12-18
Record revised 2025-03-10 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Pack of 20

Catalogue Numbers

Catalogue numbers for Empower™
Catalogue number Size Status
00884450269206 Catheter Length (cm)-130 cm In distribution
00884450491324 Catheter Length (cm)-130 cm In distribution
00884450269190 Catheter Length (cm)-130 cm In distribution
00884450493434 Catheter Length (cm)-130 cm 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
Atrieve™ Vascular Snare Kit Argon Medical Devices, Inc. 7
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

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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K193507 2020-01-17
K151497 2015-07-01
K142265 2014-11-13
K122088 2012-12-05
K092343 2009-08-07

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