Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3032745446

FEI Number

3032745446

Entity Name

Cutler Campus

City/State/Country

North Salt Lake, UT, US

Establishment Address

330 Cutler Dr, North Salt Lake, UT 84054, US

Establishment Type(s)

Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

BUNNELL INCORPORATED (Owner Number: 1719232)

Owner / Operator Contact Address

330 North Cutler Dr, --, North Salt Lake, UT 84054, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P850064

All Registered Proprietary Names

Life Pulse High Frequency Ventilator LifePulse High Frequency Ventilator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LSZ	Ventilator, High Frequency	Unknown	Class 3	N/A	2007-12-06

Official Correspondent

Therese Davy-Graham

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BUNNELL INCORPORATED

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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3013421741	VYAIRE MEDICAL, INC.	Mettawa, IL, US
2021710	ZOLL Palm Springs	Palm Springs, CA, US
3031365458	WOMED SAS	Montpellier Herault, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032745446. Last updated year: 2026. Please use registration number 3032745446 when referencing this establishment in official correspondence.