HEMASOURCE

FDA Device Registration & Listing · Salt Lake City, UT, US · Registration 1724809

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
1724809
FEI Number
3002996286
Entity Name
HEMASOURCE
City/State/Country
Salt Lake City, UT, US
Establishment Address
485 South 5700 West, Suite 400, Salt Lake City, UT 84104, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Repack or Relabel Medical Device
Owner / Operator
HemaSource, Inc. (Owner Number: 10060360)
Owner / Operator Contact Address
485 South 5700 West, Suite 400, Salt Lake City, UT 84104, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

EPI KIT Tourniquet IV Start Kit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NAB Gauze / Sponge,Nonresorbable For External Use General, Plastic Surgery Class 1 878.4014 2019-12-02

Official Correspondent

Michael Lischka

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

HemaSource, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3010611994 Source Products, Ltd. Warren, OH, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1724809. Last updated year: 2026. Please use registration number 1724809 when referencing this establishment in official correspondence.
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