C4 Development Limited

FDA Device Registration & Listing · Kwun Tong, HK · Registration 3012275122

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
3012275122
FEI Number
3012275122
Entity Name
C4 Development Limited
City/State/Country
Kwun Tong, HK
Establishment Address
Flat/Rm 1306 13/F, Winful Centre, 30 Shing Yip Street, Kwun Tong 180, HK
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Shenzhen Well Electric Co. Limited (Owner Number: 10042286)
Owner / Operator Contact Address
1-3F, No. 407 HeDongCun, HengKeng, GuanCheng Commuinty,, GuanHu Street, Longhua District, Shenzhen, CN-GD 518110, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AquilaScan WDTP-10 Drug Analyzer AquilaScan WDTP-80 Drug Analyzer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JJC Analyzer, Chemistry (Sequential Multiple, Continuous Flow) Clinical Use Clinical Chemistry Class 1 862.2150 2016-07-20

Official Correspondent

No official correspondent registered.

US Agent Details

Siobhan Sheeran Business: PAS Systems International, Inc Email: ssheeran@scramsystems.com Phone: (513) 3654126

Related Public Records

Same Entity

Shenzhen Well Electric Co. Limited
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3010160538 SHENZHEN WELL ELECTRIC CO. LIMITED Shenzhen Guangdong, CN

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K760211 Instrumentation Laboratory CO ANALYZER, GLUCOSE/UREA/CREATININE 1976-08-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012275122. Last updated year: 2026. Please use registration number 3012275122 when referencing this establishment in official correspondence.
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