Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003574195

FEI Number

3003574195

Entity Name

VASC-ALERT, LLC

City/State/Country

West Lafayette, IN, US

Establishment Address

2655 Yeager Rd., Suite 101, West Lafayette, IN 47906, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

VASC-ALERT, LLC (Owner Number: 9084139)

Owner / Operator Contact Address

2655 Yeager Rd, Suite 101, West Lafayette, IN 47906, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Vasc-Alert

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MON	System, Hemodialysis, Remote Accessories	Gastroenterology, Urology	Class 1	876.5820	2003-04-10

Official Correspondent

Douglas Curry

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VASC-ALERT, LLC

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 3003574195. Last updated year: 2026. Please use registration number 3003574195 when referencing this establishment in official correspondence.