Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2032766

FEI Number

3003502807

Entity Name

ECKERT & ZIEGLER ISOTOPE PRODUCTS

City/State/Country

VALENCIA, CA, US

Establishment Address

24937 AVENUE TIBBITTS, VALENCIA, CA 91355, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

ISOTOPE PRODUCTS LABORATORIES (Owner Number: 2020604)

Owner / Operator Contact Address

24937 AVENUE TIBBITTS, --, VALENCIA, CA 91355, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MGF-Series GF-Series HEGL-Series ISM-Series FR-Series RV-Series RR-057 Series 2600-Series SM-Series HEG-Series MED36-Series MMS-Series PHI-Series HESL-Series FM-Series NES84 Pin-Series PP-Series VQC-Series EG-0321

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IXD	Source, Calibration, Sealed, Nuclear	Radiology	Class 1	892.1400	2003-06-19
JAR	Phantom, Test-Pattern, Radionuclide	Radiology	Class 1	892.1420	2003-06-19

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ISOTOPE PRODUCTS LABORATORIES

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 2032766. Last updated year: 2026. Please use registration number 2032766 when referencing this establishment in official correspondence.