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AutoChamber — HeartLung Corporation (510(k) K240786)

AutoChamber — HeartLung Corporation (510(k) K240786) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: AutoChamber; Applicant: HeartLung Corporation; Clearance track: 510(k).

Device nameAutoChamber
ApplicantHeartLung Corporation
Clearance track510(k)
Submission numberK240786
DecisionSubstantially Equivalent
Decision date2024-10-10
Date received2024-03-22
Product codeQIH
Device class2
Medical specialtyRadiology
Applicant locationTX, US
SourceopenFDA device

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