HUIZHOU RSP TECHNOLOGY CO.,LTD

FDA Device Registration & Listing · Huizhou Guangdong, CN · Registration 3023322457

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3023322457
FEI Number
3023322457
Entity Name
HUIZHOU RSP TECHNOLOGY CO.,LTD
City/State/Country
Huizhou Guangdong, CN
Establishment Address
Building A13, Wanyang Zhongchuangcheng, Shuangyang Road, Yangqiao Town, Boluo County,, Huizhou Guangdong 516157, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Huizhou RSP Technology Co.,Ltd (Owner Number: 10085165)
Owner / Operator Contact Address
Building A13, Wanyang Zhongchuangcheng, Shuangyang Road, Yangqiao Town, Boluo County,, Huizhou, CN-GD 516157, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MNS Ventilator, Continuous, Non-Life-Supporting Anesthesiology Class 2 868.5895 2025-05-05
KMK Device, Intravascular Catheter Securement General Hospital Class 1 880.5210 2026-03-16
KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital Class 1 880.6025 2022-05-13

Official Correspondent

Lorry Luo

US Agent Details

Mike Ryan Business: Simply Shipped,LLC Email: simplyshipped.agent@gmail.com Phone: (414) 3264114

Related Public Records

Same Entity

Huizhou RSP Technology Co.,Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K033276 Resmed, Ltd. VPAP III ST-A 2004-06-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023322457. Last updated year: 2026. Please use registration number 3023322457 when referencing this establishment in official correspondence.
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