Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010677742

FEI Number

3010677742

Entity Name

PARASOL MEDICAL

City/State/Country

Buffalo Grove, IL, US

Establishment Address

1000 Asbury Dr, Suite 1, Buffalo Grove, IL 60089, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Parasol Medical LLC (Owner Number: 10046963)

Owner / Operator Contact Address

1000 Asbury Dr, Suite 1, Buffalo Grove, IL 60089, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

KMI / Monitor Bed Patient Pads Incontinence

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMI	Monitor, Bed Patient	General Hospital	Class 1	880.2400	2014-06-05

Official Correspondent

Michael Kilcran

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Parasol Medical 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 3010677742. Last updated year: 2026. Please use registration number 3010677742 when referencing this establishment in official correspondence.