LIFE SPARK MEDICAL

FDA Device Registration & Listing · Hurricane, UT, US · Registration 3040167376

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
3040167376
FEI Number
3040167376
Entity Name
LIFE SPARK MEDICAL
City/State/Country
Hurricane, UT, US
Establishment Address
2430 W 350 N, Hurricane, UT 84737, US
Establishment Type(s)
Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Life Spark Medical (Owner Number: 10094534)
Owner / Operator Contact Address
2430 West 350 North, Hurricane, UT 84737, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K250002
PMA Number
N/A

All Registered Proprietary Names

Smart Check O2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CCL Analyzer, Gas, Oxygen, Gaseous-Phase Anesthesiology Class 2 868.1720 2025-12-05

Official Correspondent

Tattiana Gray

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Life Spark Medical
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K072469 Digiflo, Inc. DIGIFLO CONCENTRATOR ANALYZER 2008-01-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3040167376. Last updated year: 2026. Please use registration number 3040167376 when referencing this establishment in official correspondence.
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