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Data / Medical devices / United States / Heathrow Scientific, LLC

Heathrow Scientific, LLC: FDA-registered device maker in Vernon Hills, IL, United States, 1 510(k) clearance

Heathrow Scientific, LLC is registered with the FDA (registration 3003510542) in Vernon Hills, IL, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 7, 1994. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3003510542
Address
440 N Fairway Dr, Vernon Hills, IL, United States, 60061
Owner or operator
Heathrow Scientific, LLC (10081165)
Roles
Specification developer
First device listed
June 23, 2022
Registered through
2026
Brand names listed
Centrifuge (Micro), Curette, surgical, general use

Devices it lists

DeviceProduct codeClassRoleSource
Centrifuges (Micro, Ultra, Refrigerated) For Clinical UseJQC1Specification developeraccessdata.fda.gov
Curette, Surgical, General UseFZS1Specification developeraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 7, 1994K932493SURGICAL CURETTEFZSSubstantially EquivalentWhitney Products, Inc.accessdata.fda.gov

Compare with other makers

Updated January 7, 1994. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.