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ORAMOIST — Quantum, Inc. (510(k) K122663)

ORAMOIST — Quantum, Inc. (510(k) K122663) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: ORAMOIST; Applicant: Quantum, Inc.; Clearance track: 510(k).

Device nameORAMOIST
ApplicantQuantum, Inc.
Clearance track510(k)
Submission numberK122663
DecisionSubstantially Equivalent
Decision date2013-05-30
Date received2012-08-31
Product codeLFD
Device classU
Medical specialtyUnknown
Applicant locationOH, US
SourceopenFDA device

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