INDUSTRIAL SOURCE

FDA Device Registration & Listing · Portland, OR, US · Registration 3009837363

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
3009837363
FEI Number
3009837363
Entity Name
INDUSTRIAL SOURCE
City/State/Country
Portland, OR, US
Establishment Address
6330 SE 101st Ave, Portland, OR 97266, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Industrial Source (Owner Number: 10056965)
Owner / Operator Contact Address
6330 SE 101st Ave, Portland, OR 97266, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Anaerobic Mixture, Clinical Blood Gas Mixture, Lung Diffusion Mixture, Laser Mixture, Calibration Mixture

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BXK Gas, Calibration (Specified Concentration) Anesthesiology Class 1 868.6400 2018-02-05

Official Correspondent

Pamela Jones

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Industrial Source
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 3009837363. Last updated year: 2026. Please use registration number 3009837363 when referencing this establishment in official correspondence.
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