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Data / Medical devices / United States / Aquilo Sports L.L.C.

Aquilo Sports L.L.C.: FDA-registered device maker in Louisville, KY, United States, 1 510(k) clearance

Aquilo Sports L.L.C. is registered with the FDA (registration 3019849074) in Louisville, KY, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 4, 2022. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3019849074
Address
214 S 8th St Ste 300, Louisville, KY, United States, 40202
Owner or operator
Aquilo Sports L.L.C. (10082395)
Roles
Repackager or relabeler, Specification developer
First device listed
July 21, 2021
Registered through
2026
Brand names listed
Aquilo Sports CCT1500 System, Aquilo Sports CT1000

Devices it lists

DeviceProduct codeClassRoleSource
Massager, Powered Inflatable TubeIRP2Repackager or relabeler, Specification developeraccessdata.fda.gov
Pack, Hot Or Cold, Water CirculatingILO2Specification 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
November 4, 2022K223164Aquilo Sports CCT1500 SystemIRPSubstantially EquivalentAquilo Sports, LLCaccessdata.fda.gov

Compare with other makers

Updated November 4, 2022. 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.