Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010145926

FEI Number

3010145926

Entity Name

CHONGQING PSK-HEALTH SCI-TECH DEVELOPMENT CO., LTD

City/State/Country

Chongqing, CN

Establishment Address

No. 3-2, 4-1, 4-2, 4th Building, Gangcheng Donghuan Road No.5, Jiangbei District, Chongqing 400026, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Chongqing PSK-Health Sci-Tech Development CO.,Ltd (Owner Number: 10046049)

Owner / Operator Contact Address

No. 3-2, 4-1, 4-2, 4th Building, Gangcheng Donghuan Road No.5, Jiangbei District, Chongqing, CN-CQ 400026, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K130439

PMA Number

N/A

All Registered Proprietary Names

Air-bag Type Sequential External Counter-pulsation Device,PECP/TI Air-bag Type Sequential External Counter-pulsation Device,PECP/TM

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DRN	Device, Counter-Pulsating, External	Cardiovascular	Class 2	870.5225	2014-01-28

Official Correspondent

Fang Sun

US Agent Details

Thomas Tang Business: Shenzhen Joyantech Consulting Co., Ltd. Email: usagent@cefda.com Phone: (631) 7511103

Related Public Records

Same Entity

Chongqing PSK-Health Sci-Tech Development CO.,Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010145926. Last updated year: 2026. Please use registration number 3010145926 when referencing this establishment in official correspondence.