Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1120044

FEI Number

1000029774

Entity Name

RICHARDSON ELECTRONICS

City/State/Country

LAFOX, IL, US

Establishment Address

40W267 KESLINGER ROAD, LAFOX, IL 60147, US

Establishment Type(s)

Remanufacture Medical Device,Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Richardson Electronics (Owner Number: 9041397)

Owner / Operator Contact Address

40W267 KESLINGER RD., P.O. Box 393, Lafox, IL 60147, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ALTA750 ALTA750G

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ITY	Assembly, Tube Housing, X-Ray, Diagnostic	Radiology	Class 1	892.1760	2018-02-27

Official Correspondent

Julie Warren

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Richardson Electronics

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 1120044. Last updated year: 2026. Please use registration number 1120044 when referencing this establishment in official correspondence.