Westec Plastics Corporation

FDA Device Registration & Listing · Livermore, CA, US · Registration 3005288662

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
3005288662
FEI Number
3005288662
Entity Name
Westec Plastics Corporation
City/State/Country
Livermore, CA, US
Establishment Address
6757 Las Positas Rd Ste A, Livermore, CA 94551, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
QA Manager (Owner Number: 10091936)
Owner / Operator Contact Address
6757 Las Positas Rd., Livermore, CA 94550, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Intellisep Cartridge

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QUT Deformability Cytometry For Sepsis Risk Assessment Microbiology Class 2 866.3215 2024-11-18

Official Correspondent

Lucero Castro

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

QA Manager
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 3005288662. Last updated year: 2026. Please use registration number 3005288662 when referencing this establishment in official correspondence.
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