Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006097795

FEI Number

3006097795

Entity Name

FINK ENGINEERING PTY LTD

City/State/Country

Laverton North Victoria, AU

Establishment Address

2/26 Westside Drive, Laverton North Victoria 3026, AU

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

FINK ENGINEERING PTY LTD (Owner Number: 9056584)

Owner / Operator Contact Address

2/26 Westside Drive, --, Laverton North, AU-VIC 3026, AU

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K240569

PMA Number

N/A

All Registered Proprietary Names

SL8 DL8 CILITY TL20 HYPERBARIC OXYGEN TREATMENT FA Fink Hyperbaric Chamber

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CBF	Chamber, Hyperbaric	Anesthesiology	Class 2	868.5470	2006-10-03
CBF	Chamber, Hyperbaric	Anesthesiology	Class 2	868.5470	2024-12-18

Official Correspondent

Eric Fink

US Agent Details

Dana Coggin Business: QUALITY & REGULATORY HELP, LLC. Email: Dana@Qrahelp.com Phone: (715) 3605401

Related Public Records

Same Entity

FINK ENGINEERING PTY LTD

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 3006097795. Last updated year: 2026. Please use registration number 3006097795 when referencing this establishment in official correspondence.