LIFESOUTH COMMUNITY BLOOD CENTERS

FDA Device Registration & Listing · Gainesville, FL, US · Registration 3003707120

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
3003707120
FEI Number
3003707120
Entity Name
LIFESOUTH COMMUNITY BLOOD CENTERS
City/State/Country
Gainesville, FL, US
Establishment Address
4039 W Newberry Rd, Gainesville, FL 32607, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LifeSouth Community Blood Centers (Owner Number: 10038488)
Owner / Operator Contact Address
4039 Newberry Road, Gainesville, FL 32607, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
BK090064
PMA Number
N/A

All Registered Proprietary Names

Integrated Blood Bank Information System, Version 4 (IBBIS) IBBIS version 1 IBBIS version 2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MMH Blood Establishment Computer Software And Accessories Hematology Class 2 864.9165 2019-07-03
MMH Blood Establishment Computer Software And Accessories Hematology Class 2 864.9165 2011-10-18
MMH Blood Establishment Computer Software And Accessories Hematology Class 2 864.9165 2011-10-18

Official Correspondent

Phuc Huynh

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LifeSouth Community Blood Centers
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3009166014 KEDRION S.P.A. Barga (Castelvecchio Pascoli) Lucca, IT
3006129391 WellSky Corporation. - Headquarters Overland Park, KS, US
3017199812 GPI USA, INC. Houston, TX, US
3020696801 CieloWorks Austin, TX, US
1058332 SCC SOFT COMPUTER CLEARWATER, FL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003707120. Last updated year: 2026. Please use registration number 3003707120 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.