Calf Cuff, XX-Large

Catalogue number Model Lumenair, listed by Vasomedical, Inc., United States, under Device, Counter-Pulsating, External. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (2), Chongqing (1).

Chinese manufacturers registered for FDA product code DRN
Manufacturer City Province Registered as Device types
Vamed Medical Instrument Co., Ltd. Foshan Guangdong Manufacturer 1
Chongqing PSK-Health SCI-Tech Development Co., Ltd. Chongqing Chongqing Manufacturer 1
Omay(Guangzhou) MED Technologies Co., Ltd. Guangzhou Guangdong Repacker / relabeller 1

Record

Regulatory record for Calf Cuff, XX-Large
Listed by Vasomedical, Inc., United States
FDA product code DRN
Device type Device, Counter-Pulsating, External
Device class Class 2
Regulation 21 CFR 870.5225
Establishment Manufacturer
510(k) K033617
Record published 2016-11-29
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only

Catalogue Numbers

Catalogue numbers for Calf Cuff, XX-Large
Catalogue number Size Status
Model Lumenair In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Vasomedical™Lumenair™ Eecp® Therapy System Vasomedical, Inc. 2
Vasomedical™ AngioNew -V Eecp® Therapy System Vasomedical, Inc. 2
Vasomedical™ AngioNew -VI Eecp® Therapy System Vasomedical, Inc. 2
PSK, Air-bag Type Sequential External Counter-pulsation Device Chongqing PSK-Health SCI-Tech Development Co., Ltd. 2
ECP PSK Chongqing PSK-Health SCI-Tech Development Co., Ltd. 2
Hose, Single, Upper Thigh (Lumenair™) Vasomedical, Inc. 1
Z-Fold ECG Paper, 147 ft. (Models TS3, and TS4 and Lumenair™) Vasomedical, Inc. 1
RejuvaHeart North American ECP Inc. 1
Calf Cuff, X-Small Vasomedical, Inc. 1
Bladder Set, Medium Vasomedical, Inc. 1
Nu Prep Gel, 4 oz (3 PK) Vasomedical, Inc. 1
Hose Single, (250mm) (AngioNew® VI) Vasomedical, Inc. 1

Showing 12 of 67. All products under Device, Counter-Pulsating, External

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K033617 2004-03-01
K020857 2002-06-14
K003469 2000-12-06

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