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Data / Medical devices / United States / Q30 Sports Science, LLC

Q30 Sports Science, LLC: FDA-registered device maker in Norwalk, CT, United States, 1 510(k) clearance

Q30 Sports Science, LLC is registered with the FDA (registration 3021373862) in Norwalk, CT, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 26, 2021. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3021373862
Address
50 Washington Street Suite 600E, Norwalk, CT, United States, 06854
Owner or operator
Q30 Sports Science, LLC (10083979)
Roles
Specification developer
First device listed
January 5, 2022
Registered through
2026
Brand names listed
Q-Collar

Devices it lists

DeviceProduct codeClassRoleSource
External Compression Device For Internal Jugular Vein CompressionQNX2Specification 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
February 26, 2021DEN200017Q-CollarQNXUnknownQ30 Sports Science, LLCaccessdata.fda.gov

Updated February 26, 2021. 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.