LASKO PRODUCTS LLC

FDA Device Registration & Listing · West Chester, PA, US · Registration 1000190272

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
1000190272
FEI Number
1000190272
Entity Name
LASKO PRODUCTS LLC
City/State/Country
West Chester, PA, US
Establishment Address
820 Lincoln avenue, West Chester, PA 19380, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Lasko Products LLC (Owner Number: 10080646)
Owner / Operator Contact Address
820 Lincoln avenue, West Chester, PA 19380, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Lasko

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KFZ Humidifier, Non-Direct Patient Interface (Home-Use) Anesthesiology Class 1 868.5460 2021-02-17

Official Correspondent

Parvathi Kodandaraman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Lasko Products LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000190272. Last updated year: 2026. Please use registration number 1000190272 when referencing this establishment in official correspondence.
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