BUOY SOFTWARE LLC

FDA Device Registration & Listing · Austin, TX, US · Registration 3030064535

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
3030064535
FEI Number
3030064535
Entity Name
BUOY SOFTWARE LLC
City/State/Country
Austin, TX, US
Establishment Address
811 Barton Springs Rd Ste 510, Austin, TX 78704, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Buoy Software (Owner Number: 10089333)
Owner / Operator Contact Address
811 Barton Springs Road, Suite 510, Austin, TX 78704, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
BK261333
PMA Number
N/A

All Registered Proprietary Names

Blood Product Questionnaire Module Blood Product Questionnaire Module v2

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 2023-11-29
MMH Blood Establishment Computer Software And Accessories Hematology Class 2 864.9165 2026-06-12

Official Correspondent

Christina Miracle

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Buoy Software
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 3030064535. Last updated year: 2026. Please use registration number 3030064535 when referencing this establishment in official correspondence.
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